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Minocycline Hydrochloride - 65862-558-30 - (Minocycline Hydrochloride)

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Drug Information of Minocycline Hydrochloride

Product NDC: 65862-558
Proprietary Name: Minocycline Hydrochloride
Non Proprietary Name: Minocycline Hydrochloride
Active Ingredient(s): 135    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: 65862-558
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA202261
Marketing Category: ANDA
Start Marketing Date: 20121119

Package Information of Minocycline Hydrochloride

Package NDC: 65862-558-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-558-30)

NDC Information of Minocycline Hydrochloride

NDC Code 65862-558-30
Proprietary Name Minocycline Hydrochloride
Package Description 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-558-30)
Product NDC 65862-558
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 20121119
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 135
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocycline Hydrochloride


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