Minocin - 16781-403-50 - (MINOCYCLINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of Minocin

Product NDC: 16781-403
Proprietary Name: Minocin
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 Minocin

Product NDC: 16781-403
Labeler Name: Onset Dermatologics, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050649
Marketing Category: NDA
Start Marketing Date: 20130507

Package Information of Minocin

Package NDC: 16781-403-50
Package Description: 50 CAPSULE in 1 BOTTLE (16781-403-50)

NDC Information of Minocin

NDC Code 16781-403-50
Proprietary Name Minocin
Package Description 50 CAPSULE in 1 BOTTLE (16781-403-50)
Product NDC 16781-403
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MINOCYCLINE HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130507
Marketing Category Name NDA
Labeler Name Onset Dermatologics, LLC
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Minocin


General Information