# Ibuprofen

NDC: 50844-921
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: 19880524
Marketing ended: 20260831
FDA application: ANDA075010

## 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:"50844-921"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-921
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3e6bc53e-9ab1-444c-b555-a85df5d83e68