# Famotidine

NDC: 21130-033
Generic name: Famotidine
Labeler / Manufacturer: Better Living Brands, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230908

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:"21130-033"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=21130-033
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6f0230c-44fb-6c36-e053-6394a90ac43e