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Denavir
Denavir - 49349-742-01 - (penciclovir)
Drug Information of Denavir
| Product NDC: | 49349-742 |
| Proprietary Name: | Denavir |
| Non Proprietary Name: | penciclovir |
| Active Ingredient(s): | 10 mg/g & nbsp; penciclovir |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Denavir
| Product NDC: | 49349-742 |
| Labeler Name: | REMEDYREPACK INC. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020629 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130611 |
Package Information of Denavir
| Package NDC: | 49349-742-01 |
| Package Description: | 5 g in 1 TUBE (49349-742-01) |
NDC Information of Denavir
| NDC Code | 49349-742-01 |
| Proprietary Name | Denavir |
| Package Description | 5 g in 1 TUBE (49349-742-01) |
| Product NDC | 49349-742 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | penciclovir |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130611 |
| Marketing Category Name | NDA |
| Labeler Name | REMEDYREPACK INC. |
| Substance Name | PENCICLOVIR |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient] |
