# DUAL ACTION BACK PAIN RELIEVER

NDC: 79481-0152
Generic name: acetaminophen, ibuprofen
Labeler / Manufacturer: Meijer, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260305

FDA application: ANDA214836

## Active ingredients

- ACETAMINOPHEN: 250 mg/1
- IBUPROFEN: 125 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"79481-0152"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=79481-0152
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8d9a0c56-ef22-45a6-8b1d-d2b2f3247210