FAMCICLOVIR
- Product NDC
- 60687-103
- 11-digit product format
- 606870103
- Labeler code
- 60687
- Product ID
- 60687-103_864765dd-5213-c5bf-e053-2991aa0a70bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FAMCICLOVIR
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA091480
- Marketing category
- ANDA
- Marketing start
- 2015-03-31
- Marketing end
- 2020-05-31
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record