Minocin - 14290-501-88 - (minocycline hydrochloride)

Alphabetical Index


Drug Information of Minocin

Product NDC: 14290-501
Proprietary Name: Minocin
Non Proprietary Name: minocycline hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   minocycline hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, COATED PELLETS
Coding System: National Drug Codes(NDC)

Labeler Information of Minocin

Product NDC: 14290-501
Labeler Name: Triax Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050649
Marketing Category: NDA
Start Marketing Date: 20070901

Package Information of Minocin

Package NDC: 14290-501-88
Package Description: 100 CAPSULE, COATED PELLETS in 1 BOTTLE (14290-501-88)

NDC Information of Minocin

NDC Code 14290-501-88
Proprietary Name Minocin
Package Description 100 CAPSULE, COATED PELLETS in 1 BOTTLE (14290-501-88)
Product NDC 14290-501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name minocycline hydrochloride
Dosage Form Name CAPSULE, COATED PELLETS
Route Name ORAL
Start Marketing Date 20070901
Marketing Category Name NDA
Labeler Name Triax Pharmaceuticals, LLC
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocin


General Information