ACZONE - 0023-3670-90 - (dapsone)

Alphabetical Index


Drug Information of ACZONE

Product NDC: 0023-3670
Proprietary Name: ACZONE
Non Proprietary Name: dapsone
Active Ingredient(s): 50    mg/g & nbsp;   dapsone
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of ACZONE

Product NDC: 0023-3670
Labeler Name: Allergan, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021794
Marketing Category: NDA
Start Marketing Date: 20090624

Package Information of ACZONE

Package NDC: 0023-3670-90
Package Description: 1 TUBE in 1 CARTON (0023-3670-90) > 90 g in 1 TUBE

NDC Information of ACZONE

NDC Code 0023-3670-90
Proprietary Name ACZONE
Package Description 1 TUBE in 1 CARTON (0023-3670-90) > 90 g in 1 TUBE
Product NDC 0023-3670
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dapsone
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20090624
Marketing Category Name NDA
Labeler Name Allergan, Inc.
Substance Name DAPSONE
Strength Number 50
Strength Unit mg/g
Pharmaceutical Classes Sulfone [EPC],Sulfones [Chemical/Ingredient]

Complete Information of ACZONE


General Information