| Product NDC: | 68462-414 |
| Proprietary Name: | Benzoyl Peroxide |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 4 g/100g & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68462-414 |
| Labeler Name: | Glenmark Generics Inc., USA |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20090130 |
| Package NDC: | 68462-414-38 |
| Package Description: | 170 g in 1 TUBE (68462-414-38) |
| NDC Code | 68462-414-38 |
| Proprietary Name | Benzoyl Peroxide |
| Package Description | 170 g in 1 TUBE (68462-414-38) |
| Product NDC | 68462-414 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20090130 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Glenmark Generics Inc., USA |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 4 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |