# Cabinet Pain Reliever and Fever Reducer

NDC: 68210-0026
Generic name: Ibuprofen
Labeler / Manufacturer: Spirit Pharmaceutical LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20191030

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:"68210-0026"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68210-0026
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e172a8d8-779d-4ad9-b6b0-08a198a58034