Famotidine
- Product NDC
- 0378-3040
- 11-digit product format
- 003783040
- Labeler code
- 0378
- Product ID
- 0378-3040_929c47c7-38f2-43c9-8293-77e0e8692aae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- famotidine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc
- Application
- ANDA075704
- Marketing category
- ANDA
- Marketing start
- 2001-04-16
- Marketing end
- 0000-00-00
- Substance
- FAMOTIDINE
- Active strength
- 40 mg/1
- Pharmacologic classes
- Histamine H2 Re
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record