Product NDC: | 54868-4956 |
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) |
Product NDC: | 54868-4956 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020629 |
Marketing Category: | NDA |
Start Marketing Date: | 20031113 |
Package NDC: | 54868-4956-0 |
Package Description: | 1 TUBE in 1 CARTON (54868-4956-0) > 1.5 g in 1 TUBE |
NDC Code | 54868-4956-0 |
Proprietary Name | Denavir |
Package Description | 1 TUBE in 1 CARTON (54868-4956-0) > 1.5 g in 1 TUBE |
Product NDC | 54868-4956 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | penciclovir |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20031113 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, 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] |