# Famotidine

NDC: 69842-063
Generic name: Famotidine
Labeler / Manufacturer: CVS Pharmacy, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200203

FDA application: ANDA206531

## Active ingredients

- FAMOTIDINE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69842-063"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69842-063
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7357f67e-0fc6-4555-aa8b-1df09cba9feb