# Ibuprofen

NDC: 51672-1385
Generic name: Ibuprofen
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20170623

FDA application: ANDA209204

## 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:"51672-1385"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1385
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a8b46ae5-67bc-494d-850e-b4e4ed5a33b3