# pain relief

NDC: 79481-3000
Generic name: Ibuprofen
Labeler / Manufacturer: Meijer, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240207

FDA application: ANDA072096

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"79481-3000"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79481-3000
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1f965703-3262-4dd1-b4f8-6341786553b1