# Ibuprofen

NDC: 50844-392
Generic name: ibuprofen
Labeler / Manufacturer: L.N.K. International, Inc.
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50844-392"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-392
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=027ded51-aa01-6619-3938-c8162a421cf3