Benzaclin - 0187-5190-35 - (Clindamycin phosphate and benzoyl peroxide)

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Drug Information of Benzaclin

Product NDC: 0187-5190
Proprietary Name: Benzaclin
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 Benzaclin

Product NDC: 0187-5190
Labeler Name: Valeant Pharmaceuticals North America LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050756
Marketing Category: NDA
Start Marketing Date: 20130531

Package Information of Benzaclin

Package NDC: 0187-5190-35
Package Description: 1 BOTTLE, PUMP in 1 CARTON (0187-5190-35) > 35 g in 1 BOTTLE, PUMP

NDC Information of Benzaclin

NDC Code 0187-5190-35
Proprietary Name Benzaclin
Package Description 1 BOTTLE, PUMP in 1 CARTON (0187-5190-35) > 35 g in 1 BOTTLE, PUMP
Product NDC 0187-5190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clindamycin phosphate and benzoyl peroxide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20130531
Marketing Category Name NDA
Labeler Name Valeant Pharmaceuticals North America LLC
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 Benzaclin


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