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Minocycline Hydrochloride - 42291-620-50 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 42291-620
Proprietary Name: Minocycline Hydrochloride
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 100    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: 42291-620
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065062
Marketing Category: ANDA
Start Marketing Date: 20110726

Package Information of Minocycline Hydrochloride

Package NDC: 42291-620-50
Package Description: 500 CAPSULE in 1 BOTTLE (42291-620-50)

NDC Information of Minocycline Hydrochloride

NDC Code 42291-620-50
Proprietary Name Minocycline Hydrochloride
Package Description 500 CAPSULE in 1 BOTTLE (42291-620-50)
Product NDC 42291-620
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110726
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline Hydrochloride


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