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Tetracycline Hydrochloride - 52959-336-40 - (Tetracycline Hydrochloride)

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Drug Information of Tetracycline Hydrochloride

Product NDC: 52959-336
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: 52959-336
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060704
Marketing Category: ANDA
Start Marketing Date: 20100323

Package Information of Tetracycline Hydrochloride

Package NDC: 52959-336-40
Package Description: 40 CAPSULE in 1 BOTTLE, PLASTIC (52959-336-40)

NDC Information of Tetracycline Hydrochloride

NDC Code 52959-336-40
Proprietary Name Tetracycline Hydrochloride
Package Description 40 CAPSULE in 1 BOTTLE, PLASTIC (52959-336-40)
Product NDC 52959-336
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tetracycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100323
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, 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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