# Famotidine

NDC: 72036-026
Generic name: Famotidine
Labeler / Manufacturer: Harris Teeter
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160426

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:"72036-026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72036-026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc548297-7646-4dbf-bfc5-65f2bc629676