# Famotidine

NDC: 51655-102
Generic name: Famotidine
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140825

FDA application: ANDA075511

## Active ingredients

- FAMOTIDINE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-102"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-102
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=03503cd5-bd8e-4bff-b90d-1a71c5225b91