# dual action pain reliever

NDC: 83324-178
Generic name: Acetaminophen and Ibuprofen
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20241003

FDA application: ANDA216999

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83324-178"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83324-178
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=23994b21-cbc2-5a34-e063-6394a90acfdf