# Advil

NDC: 0573-0134
Generic name: ibuprofen sodium
Labeler / Manufacturer: Haleon US Holdings LLC
Product type: HUMAN OTC DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20130708

FDA application: NDA201803

## Active ingredients

- IBUPROFEN SODIUM: 256 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0573-0134"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0573-0134
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5be198b8-396e-4b44-8819-e2e3b5d2ad0e