50967-219 NDC - NESTABS (MULTI-VITAMIN/MINERAL SUPPLEMENT WITH SODIUM ASCORBATE, CHOLECALCIFEROL, DI-ALPHA-TOCOPHERYL ACETATE, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HCL, FOLIC ACID, CYANOCOBALAMIN, CALCIUM FORMATE, CALCIUM CARBONATE, FERROUS (II) BIS-GLYCINATE CHELATE, POTASSIUM IODIDE, ZINC OXIDE, AND CHOLINE BITARTRATE)

Drug Information

Product NDC: 50967-219
Proprietary Name: NESTABS
Non Proprietary Name: Multi-vitamin/Mineral Supplement with Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous (II) bis-Glycinate Chelate, Potassium Iodide, Zinc Oxide, and Choline Bitartrate
Active Ingredient(s): 30 [iU]/1 .ALPHA.-TOCOPHEROL ACETATE, D-; 45 mg/1 CALCIUM CARBONATE; 155 mg/1 CALCIUM FORMATE; 450 [iU]/1 CHOLECALCIFEROL; 55 mg/1 CHOLINE BITARTRATE; 10 ug/1 CYANOCOBALAMIN; 32 mg/1 FERROUS BISGLYCINATE; 1 mg/1 FOLIC ACID; 20 mg/1 NIACINAMIDE; 100 ug/1 POTASSIUM IODIDE; 50 mg/1 PYRIDOXINE HYDROCHLORIDE; 3 mg/1 RIBOFLAVIN; 120 mg/1 SODIUM ASCORBATE; 3 mg/1 THIAMINE MONONITRATE; 10 mg/1 ZINC OXIDE
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Pharmacy Class(es): Analogs/Derivatives [Chemical/Ingredient]; Ascorbic Acid [CS]; Blood Coagulation Factor [EPC]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calcium [CS]; Cations; Divalent [CS]; Cations; Divalent [CS]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Increased Coagulation Factor Activity [PE]; Increased Coagulation Factor Activity [PE]; Phosphate Binder [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Phosphate Chelating Activity [MoA]; Vitamin B 12 [CS]; Vitamin B 6 [Chemical/Ingredient]; Vitamin B12 [EPC]; Vitamin B6 Analog [EPC]; Vitamin C [EPC]; Vitamin D [CS]; Vitamin D [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	WOMENS CHOICE PHARMACEUTICALS LLC
Product Type:	HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED DRUG OTHER
Start Marketing Date:	2/1/2011

Package Information

No.	Package Code	Package Description	Billing Unit
1	50967-219-90	1 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50967-219-90)	EA

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	50967-219	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	HUMAN PRESCRIPTION DRUG	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.
PROPRIETARY NAME	NESTABS	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
PROPRIETARY NAME SUFFIX	Prenatal Multi-vitamin/Mineral Supplement	A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
NON PROPRIETARY NAME	Multi-vitamin/Mineral Supplement with Sodium Ascorbate, Cholecalciferol, di-alpha-Tocopheryl Acetate, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine HCL, Folic Acid, Cyanocobalamin, Calcium Formate, Calcium Carbonate, Ferrous (II) bis-Glycinate Chelate, Potassium Iodide, Zinc Oxide, and Choline Bitartrate	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	TABLET, FILM COATED	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	2/1/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	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	WOMENS CHOICE PHARMACEUTICALS LLC	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	.ALPHA.-TOCOPHEROL ACETATE, D-; CALCIUM CARBONATE; CALCIUM FORMATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CYANOCOBALAMIN; FERROUS BISGLYCINATE; FOLIC ACID; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC OXIDE	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; 45; 155; 450; 55; 10; 32; 1; 20; 100; 50; 3; 120; 3; 10
ACTIVE INGRED UNIT	[iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1
PHARM CLASSES	Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Cations, Divalent [CS], Cations, Divalent [CS], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient], Vitamin B12 [EPC], Vitamin B6 Analog [EPC], Vitamin C [EPC], Vitamin D [CS], Vitamin D [EPC]

Drug Information

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Package Information

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