# Ibuprofen

NDC: 72090-070
Generic name: Ibuprofen
Labeler / Manufacturer: Pioneer Life Sciences, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260729

FDA application: ANDA079129

## 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:"72090-070"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72090-070
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8abd74a4-ad33-4c10-b677-acb469f815e6