# Famotidine

NDC: 69256-002
Generic name: Famotidine
Labeler / Manufacturer: HARRIS TEETER, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220803

FDA application: ANDA206531

## Active ingredients

- FAMOTIDINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69256-002"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69256-002
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e49e087c-ee20-3174-e053-2995a90a1d09