# ibuprofen 200

NDC: 0363-1517
Generic name: Ibuprofen
Labeler / Manufacturer: Walgreen Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20211020

FDA application: ANDA077349

## 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:"0363-1517"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0363-1517
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=49a3d51d-55d1-4b80-ab7b-35c27a937cb9