0591-2475 NDC - TETRACYCLINE HYDROCHLORIDE

Drug Information

Product NDC: 0591-2475
Proprietary Name:
Non Proprietary Name: Tetracycline Hydrochloride
Active Ingredient(s): 500 mg/1 TETRACYCLINE HYDROCHLORIDE 500 mg/1 TETRACYCLINE HYDROCHLORIDE
Administration Route(s):
Dosage Form(s): CAPSULE
Pharmacy Class(es): Tetracycline-class Antimicrobial [EPC]; Tetracyclines [CS]

Labeler Information

Field Name	Field Value
Labeler Name:	Actavis Pharma, Inc.
Product Type:	DRUG FOR FURTHER PROCESSING
FDA Application Number:
Marketing Category:	DRUG FOR FURTHER PROCESSING
Start Marketing Date:	8/15/2011
End Marketing Date:	6/10/2016

Package Information

No.	Package Code	Package Description	Billing Unit
1	0591-2475-00	15480 CAPSULE in 1 BOX (0591-2475-00)
2	0591-2475-01	100 CAPSULE in 1 BOTTLE, PLASTIC (0591-2475-01)	EA
3	0591-2475-01	100 CAPSULE in 1 BOTTLE, PLASTIC (0591-2475-01)	EA
4	0591-2475-10	1000 CAPSULE in 1 BOTTLE, PLASTIC (0591-2475-10)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	0591-2475	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.
START MARKETING DATE	8/15/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	ANDA	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	Actavis Pharma, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	0591-2475	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.
START MARKETING DATE	8/15/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	ANDA	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	Actavis Pharma, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC	0591-2475	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.
START MARKETING DATE	8/15/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	DRUG FOR FURTHER PROCESSING	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	Actavis Pharma, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 12/6/2025

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