# Ibuprofen and Famotidine

NDC: 70771-1924
Generic name: Ibuprofen and Famotidine
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250601

FDA application: ANDA218684

## Active ingredients

- FAMOTIDINE: 26.6 mg/1
- IBUPROFEN: 800 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70771-1924"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1924
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24204938-0989-42ad-8ad8-89979e62d700