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Tetracycline Hydrochloride - 24236-404-02 - (TETRACYCLINE HYDROCHLORIDE)

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Drug Information of Tetracycline Hydrochloride

Product NDC: 24236-404
Proprietary Name: Tetracycline Hydrochloride
Non Proprietary Name: TETRACYCLINE HYDROCHLORIDE
Active Ingredient(s): 250    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: 24236-404
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075659
Marketing Category: ANDA
Start Marketing Date: 20120828

Package Information of Tetracycline Hydrochloride

Package NDC: 24236-404-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (24236-404-02)

NDC Information of Tetracycline Hydrochloride

NDC Code 24236-404-02
Proprietary Name Tetracycline Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (24236-404-02)
Product NDC 24236-404
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TETRACYCLINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120828
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name TETRACYCLINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Tetracycline Hydrochloride


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