Famciclovir
- Product NDC
- 50090-3337
- 11-digit product format
- 500903337
- Labeler code
- 50090
- Product ID
- 50090-3337_9098216b-e582-4e87-9088-488c7b0999ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA202438
- Marketing category
- ANDA
- Marketing start
- 2014-09-10
- Marketing end
- 0000-00-00
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record