# Ibuprofen Dye-Free

NDC: 49035-438
Generic name: Ibuprofen
Labeler / Manufacturer: Wal-Mart Stores Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20040311
Marketing ended: 20280229
FDA application: ANDA075139

## 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:"49035-438"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49035-438
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=23cb5001-6aeb-434a-b2e8-aaf8bbab9dc6