# Famotidine

NDC: 63187-723
Generic name: Famotidine
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160129

FDA application: ANDA078916

## 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:"63187-723"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-723
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9baf2596-b771-4bae-a03c-d3af6716821d