# Famotidine

NDC: 72657-113
Generic name: Famotidine
Labeler / Manufacturer: GLENMARK THERAPEUTICS INC., USA
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220601

FDA application: ANDA215822

## 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:"72657-113"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72657-113
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95f51f27-d367-4cfd-a15f-7856c9e361fb