# Famotidine

NDC: 46122-737
Generic name: Famotidine
Labeler / Manufacturer: Amerisource Bergen
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230720

FDA application: ANDA206531

## Active ingredients

- FAMOTIDINE: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46122-737"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46122-737
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d8df03ab-7c5c-4c8b-a3fb-6c6081e081e7