Famciclovir
- Product NDC
- 57237-196
- 11-digit product format
- 572370196
- Labeler code
- 57237
- Product ID
- 57237-196_7a58bb13-3fa9-457e-ad16-2de9aab7b862
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Famciclovir
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Citron Pharma LLC
- Application
- ANDA091114
- Marketing category
- ANDA
- Marketing start
- 2011-03-21
- 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
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record