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Famciclovir
Famciclovir - 0781-5621-31 - (famciclovir)
Drug Information of Famciclovir
| Product NDC: | 0781-5621 |
| Proprietary Name: | Famciclovir |
| Non Proprietary Name: | famciclovir |
| Active Ingredient(s): | 250 mg/1 & nbsp; famciclovir |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Famciclovir
| Product NDC: | 0781-5621 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020363 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 20110307 |
Package Information of Famciclovir
| Package NDC: | 0781-5621-31 |
| Package Description: | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5621-31) |
NDC Information of Famciclovir
| NDC Code | 0781-5621-31 |
| Proprietary Name | Famciclovir |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0781-5621-31) |
| Product NDC | 0781-5621 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | famciclovir |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20110307 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Sandoz Inc |
| Substance Name | FAMCICLOVIR |
| Strength Number | 250 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient] |
