Famotidine
- Product NDC
- 63629-7909
- 11-digit product format
- 636297909
- Labeler code
- 63629
- Product ID
- 63629-7909_e5d1d71e-4f49-45b5-892c-1f6570358f2d
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA075512
- Marketing category
- ANDA
- Marketing start
- 2015-01-08
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 10 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record