# IBUPROFEN

NDC: 68210-0200
Generic name: IBUPROFEN
Labeler / Manufacturer: SPIRIT PHARMACEUTICALS,LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE, LIQUID FILLED
Routes: ORAL
Marketing started: 20180410

FDA application: ANDA079205

## 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:"68210-0200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68210-0200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2810122e-3c89-49a2-8dac-db3714cb7b45