# Famotidine

NDC: 0832-6045
Generic name: Famotidine
Labeler / Manufacturer: Upsher-Smith Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20230616

FDA application: ANDA217655

## Active ingredients

- FAMOTIDINE: 40 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0832-6045"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0832-6045
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d528fadf-316f-4fea-9bec-070c01f80d64