# Ibuprofen

NDC: 68016-635
Generic name: Ibuprofen
Labeler / Manufacturer: Chain Drug Consortium
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19990301
Marketing ended: 20260731
FDA application: ANDA075139

## 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:"68016-635"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-635
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=63f270d9-244a-43a0-b472-03137b1f259f