# Ibuprofen

NDC: 69367-396
Generic name: Ibuprofen
Labeler / Manufacturer: Westminster Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240523

FDA application: ANDA202413

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"69367-396"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=69367-396
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eeb8312f-7fd9-4c4f-8264-a7e63ff1aa9d