# FAMOTIDINE

NDC: 70518-4574
Generic name: FAMOTIDINE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260216

FDA application: ANDA215630

## 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:"70518-4574"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4574
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3ab235f4-da59-4a92-ad6b-c76cf3ecd985