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Peroderm 7
Peroderm 7 - 51991-699-16 - (Benzoyl Peroxide)
Drug Information of Peroderm 7
| Product NDC: | 51991-699 |
| Proprietary Name: | Peroderm 7 |
| Non Proprietary Name: | Benzoyl Peroxide |
| Active Ingredient(s): | 70 mg/g & nbsp; Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Peroderm 7
| Product NDC: | 51991-699 |
| Labeler Name: | Breckenridge Pharmaceutical inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091215 |
Package Information of Peroderm 7
| Package NDC: | 51991-699-16 |
| Package Description: | 1 BOTTLE in 1 CARTON (51991-699-16) > 453.59 g in 1 BOTTLE |
NDC Information of Peroderm 7
| NDC Code | 51991-699-16 |
| Proprietary Name | Peroderm 7 |
| Package Description | 1 BOTTLE in 1 CARTON (51991-699-16) > 453.59 g in 1 BOTTLE |
| Product NDC | 51991-699 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Benzoyl Peroxide |
| Dosage Form Name | SOLUTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20091215 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Breckenridge Pharmaceutical inc. |
| Substance Name | BENZOYL PEROXIDE |
| Strength Number | 70 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
