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Tetracycline Hydrochloride - 0591-2235-10 - (Tetracycline Hydrochloride)

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Drug Information of Tetracycline Hydrochloride

Product NDC: 0591-2235
Proprietary Name: Tetracycline Hydrochloride
Non Proprietary Name: Tetracycline Hydrochloride
Active Ingredient(s): 500    mg/1 & nbsp;   Tetracycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Tetracycline Hydrochloride

Product NDC: 0591-2235
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061837
Marketing Category: ANDA
Start Marketing Date: 20101219

Package Information of Tetracycline Hydrochloride

Package NDC: 0591-2235-10
Package Description: 1000 CAPSULE in 1 BOTTLE, PLASTIC (0591-2235-10)

NDC Information of Tetracycline Hydrochloride

NDC Code 0591-2235-10
Proprietary Name Tetracycline Hydrochloride
Package Description 1000 CAPSULE in 1 BOTTLE, PLASTIC (0591-2235-10)
Product NDC 0591-2235
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tetracycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101219
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
Substance Name TETRACYCLINE HYDROCHLORIDE
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Tetracycline Hydrochloride


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