# Famotidine

NDC: 54257-802
Generic name: Famotidine
Labeler / Manufacturer: Magno-Humphries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160426

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:"54257-802"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54257-802
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f5d5b40e-82e5-4284-9f3f-d2c0e88f0ab9