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Erythromycin and Benzoyl Peroxide
Erythromycin and Benzoyl Peroxide - 0781-7054-49 - (Erythromycin and Benzoyl Peroxide)
Drug Information of Erythromycin and Benzoyl Peroxide
| Product NDC: | 0781-7054 |
| Proprietary Name: | Erythromycin and Benzoyl Peroxide |
| Non Proprietary Name: | Erythromycin and Benzoyl Peroxide |
| Active Ingredient(s): | & nbsp; Erythromycin and Benzoyl Peroxide |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Erythromycin and Benzoyl Peroxide
| Product NDC: | 0781-7054 |
| Labeler Name: | Sandoz |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065112 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040329 |
Package Information of Erythromycin and Benzoyl Peroxide
| Package NDC: | 0781-7054-49 |
| Package Description: | 1 KIT in 1 CARTON (0781-7054-49) * .8 g in 1 VIAL, PLASTIC (0781-8054-01) * 20 g in 1 JAR (0781-9054-22) |
NDC Information of Erythromycin and Benzoyl Peroxide
| NDC Code | 0781-7054-49 |
| Proprietary Name | Erythromycin and Benzoyl Peroxide |
| Package Description | 1 KIT in 1 CARTON (0781-7054-49) * .8 g in 1 VIAL, PLASTIC (0781-8054-01) * 20 g in 1 JAR (0781-9054-22) |
| Product NDC | 0781-7054 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Erythromycin and Benzoyl Peroxide |
| Dosage Form Name | KIT |
| Route Name | TOPICAL |
| Start Marketing Date | 20040329 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz |
| Substance Name | |
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