Famotidine
- Product NDC
- 41167-0020
- 11-digit product format
- 411670020
- Labeler code
- 41167
- Product ID
- 41167-0020_01059552-a460-47a8-bb61-df48ec3efb17
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- CHATTEM, INC.
- Application
- ANDA206531
- Marketing category
- ANDA
- Marketing start
- 2020-11-03
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 20 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record