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Minocycline Hydrochloride - 0781-5386-31 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 0781-5386
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, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Minocycline Hydrochloride

Product NDC: 0781-5386
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090422
Marketing Category: ANDA
Start Marketing Date: 20090813

Package Information of Minocycline Hydrochloride

Package NDC: 0781-5386-31
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5386-31)

NDC Information of Minocycline Hydrochloride

NDC Code 0781-5386-31
Proprietary Name Minocycline Hydrochloride
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5386-31)
Product NDC 0781-5386
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090813
Marketing Category Name ANDA
Labeler Name Sandoz 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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