# Famotidine

NDC: 60760-736
Generic name: Famotidine
Labeler / Manufacturer: ST. MARY'S MEDICAL PARK PHARMACY
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221208

FDA application: ANDA216441

## Active ingredients

- FAMOTIDINE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60760-736"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60760-736
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f175822d-7ca4-fa33-e053-2995a90ac310