# Ibuprofen

NDC: 59726-123
Generic name: Ibuprofen
Labeler / Manufacturer: P & L Development, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20230331

FDA application: ANDA202300

## 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:"59726-123"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59726-123
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1889faea-24a3-45ea-92de-8dc76b9ed5b4