# IBUPROFEN

NDC: 41226-600
Generic name: IBUPROFEN
Labeler / Manufacturer: Kroger Company
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20210612

FDA application: ANDA091239

## 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:"41226-600"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=41226-600
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bc173f1b-2e44-2c2e-e053-2a95a90a89c4