# Ibuprofen

NDC: 0904-7914
Generic name: ibuprofen
Labeler / Manufacturer: Major Pharmaceuticals
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 19990301

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:"0904-7914"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0904-7914
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a5ad1cd-e6a3-44ad-b9b8-ff9b66f390f6