# Famotidine

NDC: 27241-249
Generic name: Famotidine
Labeler / Manufacturer: Ajanta Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: FOR SUSPENSION
Routes: ORAL
Marketing started: 20220425

FDA application: ANDA217529

## Active ingredients

- FAMOTIDINE: 40 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"27241-249"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=27241-249
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a88e7069-230c-4105-ade0-a98968e18671