# IBUPROFEN

NDC: 67060-001
Generic name: IBUPROFEN 200MG
Labeler / Manufacturer: ADVANCED FIRST AID, INC.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20150409

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:"67060-001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67060-001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=564e9910-b491-4129-a4f1-68216267623b