Solodyn - 99207-463-02 - (minocycline hydrochloride)

Alphabetical Index


Drug Information of Solodyn

Product NDC: 99207-463
Proprietary Name: Solodyn
Non Proprietary Name: minocycline hydrochloride
Active Ingredient(s): 65    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: 99207-463
Labeler Name: Medicis Pharmaceutical Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050808
Marketing Category: NDA
Start Marketing Date: 20090723

Package Information of Solodyn

Package NDC: 99207-463-02
Package Description: 10 BOTTLE in 1 CARTON (99207-463-02) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE

NDC Information of Solodyn

NDC Code 99207-463-02
Proprietary Name Solodyn
Package Description 10 BOTTLE in 1 CARTON (99207-463-02) > 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product NDC 99207-463
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 20090723
Marketing Category Name NDA
Labeler Name Medicis Pharmaceutical Corp.
Substance Name MINOCYCLINE HYDROCHLORIDE
Strength Number 65
Strength Unit mg/1
Pharmaceutical Classes Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient]

Complete Information of Solodyn


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