# Famotidine

NDC: 87441-030
Generic name: Famotidine
Labeler / Manufacturer: Unit Dose Solutions, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260622

FDA application: ANDA206530

## 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:"87441-030"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87441-030
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=54d93bf1-8f9a-981b-e063-6394a90a0fde