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Minocycline Hydrochloride - 65862-211-99 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 65862-211
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: 65862-211
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065470
Marketing Category: ANDA
Start Marketing Date: 20080311

Package Information of Minocycline Hydrochloride

Package NDC: 65862-211-99
Package Description: 1000 CAPSULE in 1 BOTTLE (65862-211-99)

NDC Information of Minocycline Hydrochloride

NDC Code 65862-211-99
Proprietary Name Minocycline Hydrochloride
Package Description 1000 CAPSULE in 1 BOTTLE (65862-211-99)
Product NDC 65862-211
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20080311
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
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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