# Famotidine

NDC: 70000-0049
Generic name: Famotidine
Labeler / Manufacturer: LEADER/ CARDINAL HEALTH 110, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200404

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:"70000-0049"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70000-0049
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=78b168f1-846d-4e88-a8ee-845c41c9dcbe