41701-008 NDC - VASOPRESSIN

Drug Information

Product NDC: 41701-008
Proprietary Name:
Non Proprietary Name: Vasopressin
Active Ingredient(s): .3 g/.3g VASOPRESSIN, UNSPECIFIED1 g/g VASOPRESSIN, UNSPECIFIED1.5 g/1.5g VASOPRESSIN, UNSPECIFIED1.83 g/1.83g VASOPRESSIN, UNSPECIFIED1.85 g/1.85g VASOPRESSIN, UNSPECIFIED30 g/30g VASOPRESSIN, UNSPECIFIED1.73 g/1.73g VASOPRESSIN, UNSPECIFIED2.65 g/2.65g VASOPRESSIN, UNSPECIFIED2.7 g/2.7g VASOPRESSIN, UNSPECIFIED3.35 g/3.35g VASOPRESSIN, UNSPECIFIED9.1 g/9.1g VASOPRESSIN, UNSPECIFIED1.2 g/1.2g VASOPRESSIN, UNSPECIFIED1.8 g/1.8g VASOPRESSIN, UNSPECIFIED1.84 g/1.84g VASOPRESSIN, UNSPECIFIED3 g/3g VASOPRESSIN, UNSPECIFIED2 g/2g VASOPRESSIN, UNSPECIFIED8 g/8g VASOPRESSIN, UNSPECIFIED.8 g/.8g VASOPRESSIN, UNSPECIFIED.9 g/.9g VASOPRESSIN, UNSPECIFIED6 g/6g VASOPRESSIN, UNSPECIFIED.5 g/.5g VASOPRESSIN, UNSPECIFIED.6 g/.6g VASOPRESSIN, UNSPECIFIED
Administration Route(s):
Dosage Form(s): POWDER

Labeler Information

Field Name	Field Value
Labeler Name:	Hemmo Pharmaceuticals Pvt. Ltd
Product Type:	BULK INGREDIENT
FDA Application Number:
Marketing Category:	BULK INGREDIENT
Start Marketing Date:	3/28/2016

Package Information

No.	Package Code	Package Description
1	41701-008-30	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-30) / .6 g in 1 BOTTLE, PLASTIC (41701-008-29)
2	41701-008-32	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-32) / 3 g in 1 BOTTLE, PLASTIC (41701-008-31)
3	41701-008-34	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-34) / 6 g in 1 BOTTLE, PLASTIC (41701-008-33)
4	41701-008-36	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-36) / 9.1 g in 1 BOTTLE, PLASTIC (41701-008-35)
5	41701-008-38	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-38) / .5 g in 1 BOTTLE, PLASTIC (41701-008-37)
6	41701-008-40	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-40) / 2 g in 1 BOTTLE, PLASTIC (41701-008-39)
7	41701-008-42	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-42) / 3.35 g in 1 BOTTLE, PLASTIC (41701-008-41)
8	41701-008-44	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-44) / 8 g in 1 BOTTLE, PLASTIC (41701-008-43)
9	41701-008-46	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-46) / .8 g in 1 BOTTLE, PLASTIC (41701-008-45)
10	41701-008-48	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-48) / 1.8 g in 1 BOTTLE, PLASTIC (41701-008-47)
11	41701-008-50	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-50) / 1.73 g in 1 BOTTLE, PLASTIC (41701-008-49)
12	41701-008-52	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-52) / 1.84 g in 1 BOTTLE, PLASTIC (41701-008-51)
13	41701-008-54	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-54) / 1.83 g in 1 BOTTLE, PLASTIC (41701-008-53)
14	41701-008-56	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-56) / 1.85 g in 1 BOTTLE, PLASTIC (41701-008-55)
15	41701-008-58	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-58) / 30 g in 1 BOTTLE, PLASTIC (41701-008-57)
16	41701-008-60	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-60) / 1.2 g in 1 BOTTLE, PLASTIC (41701-008-59)
17	41701-008-62	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-62) / .3 g in 1 BOTTLE, PLASTIC (41701-008-61)
18	41701-008-64	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-64) / .9 g in 1 BOTTLE, PLASTIC (41701-008-63)
19	41701-008-66	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-66) / 2.65 g in 1 BOTTLE, PLASTIC (41701-008-65)
20	41701-008-68	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-68) / 1.5 g in 1 BOTTLE, PLASTIC (41701-008-67)
21	41701-008-70	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-70) / 2.7 g in 1 BOTTLE, PLASTIC (41701-008-69)
22	41701-008-72	1 BOTTLE, PLASTIC in 1 PACKAGE (41701-008-72) / 1 g in 1 BOTTLE, PLASTIC (41701-008-71)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.3
ACTIVE INGRED UNIT	g/.3g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1
ACTIVE INGRED UNIT	g/g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.5
ACTIVE INGRED UNIT	g/1.5g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.83
ACTIVE INGRED UNIT	g/1.83g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.85
ACTIVE INGRED UNIT	g/1.85g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	30
ACTIVE INGRED UNIT	g/30g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.73
ACTIVE INGRED UNIT	g/1.73g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	2.65
ACTIVE INGRED UNIT	g/2.65g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	2.7
ACTIVE INGRED UNIT	g/2.7g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	3.35
ACTIVE INGRED UNIT	g/3.35g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	9.1
ACTIVE INGRED UNIT	g/9.1g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.2
ACTIVE INGRED UNIT	g/1.2g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.8
ACTIVE INGRED UNIT	g/1.8g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	1.84
ACTIVE INGRED UNIT	g/1.84g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	3
ACTIVE INGRED UNIT	g/3g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	2
ACTIVE INGRED UNIT	g/2g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	8
ACTIVE INGRED UNIT	g/8g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.8
ACTIVE INGRED UNIT	g/.8g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.9
ACTIVE INGRED UNIT	g/.9g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	6
ACTIVE INGRED UNIT	g/6g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Piramal Pharma Limited	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.5
ACTIVE INGRED UNIT	g/.5g
PRODUCT NDC	41701-008	The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAME	BULK INGREDIENT	Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
NON PROPRIETARY NAME	Vasopressin	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	POWDER	The translation of the dosage form Code submitted by the firm.
START MARKETING DATE	3/28/2016	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	BULK INGREDIENT	Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAME	Hemmo Pharmaceuticals Pvt. Ltd	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	VASOPRESSIN, UNSPECIFIED	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH	.6
ACTIVE INGRED UNIT	g/.6g

41701-008 NDC - VASOPRESSIN

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