# ibuprofen

NDC: 51672-5321
Generic name: ibuprofen
Labeler / Manufacturer: TARO PHARMACEUTICALS U.S.A., INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20240815

FDA application: ANDA211666

## Active ingredients

- IBUPROFEN: 100 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-5321"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-5321
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9de61620-6750-4fb6-89a4-fe451ab8d99f