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 |