Product NDC: | 0066-0577 |
Proprietary Name: | Benzamycin Pak |
Non Proprietary Name: | erythromycin and benzoyl peroxide |
Active Ingredient(s): | 50; 30 mg/g; mg/g & nbsp; erythromycin and benzoyl peroxide |
Administration Route(s): | TOPICAL |
Dosage Form(s): | GEL |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0066-0577 |
Labeler Name: | Dermik Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050769 |
Marketing Category: | NDA |
Start Marketing Date: | 20020101 |
Package NDC: | 0066-0577-60 |
Package Description: | 60 POUCH in 1 CARTON (0066-0577-60) > .8 g in 1 POUCH |
NDC Code | 0066-0577-60 |
Proprietary Name | Benzamycin Pak |
Package Description | 60 POUCH in 1 CARTON (0066-0577-60) > .8 g in 1 POUCH |
Product NDC | 0066-0577 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | erythromycin and benzoyl peroxide |
Dosage Form Name | GEL |
Route Name | TOPICAL |
Start Marketing Date | 20020101 |
Marketing Category Name | NDA |
Labeler Name | Dermik Laboratories |
Substance Name | BENZOYL PEROXIDE; ERYTHROMYCIN |
Strength Number | 50; 30 |
Strength Unit | mg/g; mg/g |
Pharmaceutical Classes | Decreased Sebaceous Gland Activity [PE],Macrolide [EPC],Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient] |