# Famotidine

NDC: 67877-775
Generic name: Famotidine
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20230824

FDA application: ANDA216400

## 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:"67877-775"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-775
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b2228be0-472b-4e47-9910-af0bf12fde77