# Famotidine

NDC: 58602-705
Generic name: Famotidine
Labeler / Manufacturer: Aurohealth LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160426

FDA application: ANDA206531

## 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:"58602-705"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=58602-705
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=756c7234-6a63-4b1b-be36-2b1ed09e67a0