Product NDC: | 66993-949 |
Proprietary Name: | Clindamycin - Benzoyl Peroxide |
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) |
Product NDC: | 66993-949 |
Labeler Name: | Prasco Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050741 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20120627 |
Package NDC: | 66993-949-45 |
Package Description: | 1 TUBE in 1 CARTON (66993-949-45) > 45 g in 1 TUBE |
NDC Code | 66993-949-45 |
Proprietary Name | Clindamycin - Benzoyl Peroxide |
Package Description | 1 TUBE in 1 CARTON (66993-949-45) > 45 g in 1 TUBE |
Product NDC | 66993-949 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | clindamycin phosphate and benzoyl peroxide |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20120627 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Prasco Laboratories |
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] |