# Ibuprofen

NDC: 68016-813
Generic name: Ibuprofen
Labeler / Manufacturer: Chain Drug Consortium, LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20220826
Marketing ended: 20261231
FDA application: ANDA206568

## 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:"68016-813"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68016-813
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f0f01b97-e52c-4077-a4c6-c59736f4c171