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Minocycline hydrochloride - 54868-5040-1 - (Minocycline hydrochloride)

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Drug Information of Minocycline hydrochloride

Product NDC: 54868-5040
Proprietary Name: Minocycline hydrochloride
Non Proprietary Name: Minocycline hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Minocycline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Minocycline hydrochloride

Product NDC: 54868-5040
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065062
Marketing Category: ANDA
Start Marketing Date: 20050414

Package Information of Minocycline hydrochloride

Package NDC: 54868-5040-1
Package Description: 10 CAPSULE in 1 BOTTLE (54868-5040-1)

NDC Information of Minocycline hydrochloride

NDC Code 54868-5040-1
Proprietary Name Minocycline hydrochloride
Package Description 10 CAPSULE in 1 BOTTLE (54868-5040-1)
Product NDC 54868-5040
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050414
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline hydrochloride


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