BENZACLIN - 54868-6062-0 - (clindamycin phosphate and benzoyl peroxide)

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Drug Information of BENZACLIN

Product NDC: 54868-6062
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: 54868-6062
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050756
Marketing Category: NDA
Start Marketing Date: 20090827

Package Information of BENZACLIN

Package NDC: 54868-6062-0
Package Description: 1 JAR in 1 CARTON (54868-6062-0) > 6 g in 1 JAR

NDC Information of BENZACLIN

NDC Code 54868-6062-0
Proprietary Name BENZACLIN
Package Description 1 JAR in 1 CARTON (54868-6062-0) > 6 g in 1 JAR
Product NDC 54868-6062
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clindamycin phosphate and benzoyl peroxide
Dosage Form Name GEL
Route Name TOPICAL
Start Marketing Date 20090827
Marketing Category Name NDA
Labeler Name Physicians Total Care, 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 BENZACLIN


General Information