# IBUPROFEN

NDC: 0363-9594
Generic name: IBUPROFEN
Labeler / Manufacturer: WALGREENS CO.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20211015

FDA application: ANDA079174

## 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:"0363-9594"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-9594
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b8a77b7e-e161-b3ac-e053-2995a90af3e8