# Ibuprofen

NDC: 63941-210
Generic name: Ibuprofen
Labeler / Manufacturer: VALU MERCHANDISERS COMPANY
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20170601
Marketing ended: 20280430
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:"63941-210"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63941-210
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=88b3f388-46d3-4e42-98fb-0351c76a15fc