DUAC - 0145-5371-61 - (clindamycin phosphate and benzoyl peroxide)

Alphabetical Index


Drug Information of DUAC

Product NDC: 0145-5371
Proprietary Name: DUAC
Non Proprietary Name: clindamycin phosphate and benzoyl peroxide
Active Ingredient(s): 50; 10    mg/g; mg/g & nbsp;   clindamycin phosphate and benzoyl peroxide
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Coding System: National Drug Codes(NDC)

Labeler Information of DUAC

Product NDC: 0145-5371
Labeler Name: Stiefel Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050741
Marketing Category: NDA
Start Marketing Date: 20110301

Package Information of DUAC

Package NDC: 0145-5371-61
Package Description: 20 TUBE in 1 CARTON (0145-5371-61) > 5 g in 1 TUBE (0145-5371-01)

NDC Information of DUAC

NDC Code 0145-5371-61
Proprietary Name DUAC
Package Description 20 TUBE in 1 CARTON (0145-5371-61) > 5 g in 1 TUBE (0145-5371-01)
Product NDC 0145-5371
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin phosphate and benzoyl peroxide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20110301
Marketing Category Name NDA
Labeler Name Stiefel Laboratories Inc
Substance Name BENZOYL PEROXIDE; CLINDAMYCIN PHOSPHATE
Strength Number 50; 10
Strength Unit mg/g; mg/g
Pharmaceutical Classes Decreased Sebaceous Gland Activity [PE],Lincosamide Antibacterial [EPC],Lincosamides [Chemical/Ingredient]

Complete Information of DUAC


General Information