# Ibuprofen

NDC: 51655-275
Generic name: Ibuprofen
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200616

FDA application: ANDA090796

## Active ingredients

- IBUPROFEN: 800 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-275"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-275
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c20f1f4d-59b3-6bbe-e053-2a95a90abaf1