# Ibuprofen

NDC: 63868-571
Generic name: Ibuprofen
Labeler / Manufacturer: CHAIN DRUG MARKETING ASSOCIATION INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20200325
Marketing ended: 20270228
FDA application: ANDA202312

## 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:"63868-571"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63868-571
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c1cc205-b9e3-03fc-e053-2995a90aaffb