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Tetracycline Hydrochloride - 54868-0024-1 - (Tetracycline Hydrochloride)

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Drug Information of Tetracycline Hydrochloride

Product NDC: 54868-0024
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: 54868-0024
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA060704
Marketing Category: ANDA
Start Marketing Date: 19880301

Package Information of Tetracycline Hydrochloride

Package NDC: 54868-0024-1
Package Description: 40 CAPSULE in 1 BOTTLE (54868-0024-1)

NDC Information of Tetracycline Hydrochloride

NDC Code 54868-0024-1
Proprietary Name Tetracycline Hydrochloride
Package Description 40 CAPSULE in 1 BOTTLE (54868-0024-1)
Product NDC 54868-0024
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Tetracycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19880301
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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