Home > National Drug Code (NDC) > Minocycline Hydrochloride

Minocycline Hydrochloride - 0093-3167-53 - (Minocycline Hydrochloride)

Alphabetical Index


Drug Information of Minocycline Hydrochloride

Product NDC: 0093-3167
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: 0093-3167
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA063009
Marketing Category: ANDA
Start Marketing Date: 19920501

Package Information of Minocycline Hydrochloride

Package NDC: 0093-3167-53
Package Description: 50 CAPSULE in 1 BOTTLE (0093-3167-53)

NDC Information of Minocycline Hydrochloride

NDC Code 0093-3167-53
Proprietary Name Minocycline Hydrochloride
Package Description 50 CAPSULE in 1 BOTTLE (0093-3167-53)
Product NDC 0093-3167
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Minocycline Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19920501
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA 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


General Information