Famciclovir
- Product NDC
- 71335-2936
- 11-digit product format
- 713352936
- Labeler code
- 71335
- Product ID
- 71335-2936_f8a739c5-2fac-409e-a788-85300bdad173
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA201022
- Marketing category
- ANDA
- Marketing start
- 2012-01-13
- Substance
- FAMCICLOVIR
- Active strength
- 500 mg/1
- Pharmacologic classes
- DNA Polymerase Inhibitors [MoA], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| QIC03ANI02 | FAMCICLOVIR | 104227-87-4 | FAMCICLOVIR |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2936-1 | 71335293601 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2936-1) | 2025-10-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Famciclovir | Bryant Ranch Prepack | 2025-10-28 | HUMAN PRESCRIPTION DRUG LABEL | 1 |