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Minocycline Hydrochloride - 55154-8289-0 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 55154-8289
Proprietary Name: Minocycline Hydrochloride
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 50    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: 55154-8289
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063011
Marketing Category: ANDA
Start Marketing Date: 19920501

Package Information of Minocycline Hydrochloride

Package NDC: 55154-8289-0
Package Description: 10 POUCH in 1 BAG (55154-8289-0) > 1 CAPSULE in 1 POUCH

NDC Information of Minocycline Hydrochloride

NDC Code 55154-8289-0
Proprietary Name Minocycline Hydrochloride
Package Description 10 POUCH in 1 BAG (55154-8289-0) > 1 CAPSULE in 1 POUCH
Product NDC 55154-8289
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19920501
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline Hydrochloride


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