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Minocycline Hydrochloride - 0378-4297-93 - (minocycline hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 0378-4297
Proprietary Name: Minocycline Hydrochloride
Non Proprietary Name: minocycline hydrochloride
Active Ingredient(s): 90    mg/1 & nbsp;   minocycline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Minocycline Hydrochloride

Product NDC: 0378-4297
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090911
Marketing Category: ANDA
Start Marketing Date: 20120829

Package Information of Minocycline Hydrochloride

Package NDC: 0378-4297-93
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4297-93)

NDC Information of Minocycline Hydrochloride

NDC Code 0378-4297-93
Proprietary Name Minocycline Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-4297-93)
Product NDC 0378-4297
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name minocycline hydrochloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20120829
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 90
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline Hydrochloride


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