Solodyn - 99207-462-01 - (minocycline hydrochloride)

Alphabetical Index


Drug Information of Solodyn

Product NDC: 99207-462
Proprietary Name: Solodyn
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 Solodyn

Product NDC: 99207-462
Labeler Name: Medicis Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050808
Marketing Category: NDA
Start Marketing Date: 20060508

Package Information of Solodyn

Package NDC: 99207-462-01
Package Description: 20 BLISTER PACK in 1 CARTON (99207-462-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

NDC Information of Solodyn

NDC Code 99207-462-01
Proprietary Name Solodyn
Package Description 20 BLISTER PACK in 1 CARTON (99207-462-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product NDC 99207-462
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 20060508
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 135
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Solodyn


General Information