# Ibuprofen

NDC: 80425-0537
Generic name: ibuprofen
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250805

FDA application: ANDA078329

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0537"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0537
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3b9fdc48-c071-4e2c-e063-6294a90a679f