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Minocin Kit - 14290-571-98 - (minocycline hydrochloride)

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Drug Information of Minocin Kit

Product NDC: 14290-571
Proprietary Name: Minocin Kit
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 Kit

Product NDC: 14290-571
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 Kit

Package NDC: 14290-571-98
Package Description: 1 BOTTLE in 1 CARTON (14290-571-98) > 60 CAPSULE, COATED PELLETS in 1 BOTTLE

NDC Information of Minocin Kit

NDC Code 14290-571-98
Proprietary Name Minocin Kit
Package Description 1 BOTTLE in 1 CARTON (14290-571-98) > 60 CAPSULE, COATED PELLETS in 1 BOTTLE
Product NDC 14290-571
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 Kit


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