# ibuprofen

NDC: 87441-043
Generic name: Ibuprofen
Labeler / Manufacturer: Unit Dose Solutions, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260625

FDA application: ANDA072096

## Active ingredients

- IBUPROFEN: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"87441-043"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87441-043
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=551535ce-eab0-bb13-e063-6294a90a2070