# Famotidine

NDC: 55681-341
Generic name: Famotidine
Labeler / Manufacturer: TWIN MED LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220128

FDA application: ANDA215822

## Active ingredients

- FAMOTIDINE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55681-341"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55681-341
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f7f1bb4e-df0d-8a7b-e053-6294a90a9c47