# Famotidine

NDC: 69842-924
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: 20210628

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:"69842-924"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69842-924
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c4e35c7e-5c2f-4252-e053-2a95a90a8268