DYNACIN - 49884-097-01 - (Minocycline Hydrochloride)

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Drug Information of DYNACIN

Product NDC: 49884-097
Proprietary Name: DYNACIN
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 75    mg/1 & nbsp;   Minocycline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of DYNACIN

Product NDC: 49884-097
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065131
Marketing Category: ANDA
Start Marketing Date: 20110620

Package Information of DYNACIN

Package NDC: 49884-097-01
Package Description: 100 TABLET in 1 BOTTLE (49884-097-01)

NDC Information of DYNACIN

NDC Code 49884-097-01
Proprietary Name DYNACIN
Package Description 100 TABLET in 1 BOTTLE (49884-097-01)
Product NDC 49884-097
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110620
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical, Inc.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of DYNACIN


General Information