# FAMOTIDINE

NDC: 59651-701
Generic name: FAMOTIDINE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SUSPENSION
Routes: ORAL
Marketing started: 20250709

FDA application: ANDA219091

## 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:"59651-701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=18066b80-1ec6-4092-80d9-70adb0ecac85