# Ibuprofen and Famotidine

NDC: 80425-0587
Generic name: Ibuprofen and Famotidine
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260618

FDA application: ANDA218684

## Active ingredients

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

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0587"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0587
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=548c705e-4094-fc6f-e063-6394a90a3426