# Ibuprofen

NDC: 50844-352
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50844-352"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50844-352
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8ebe3e16-b7ae-d333-6671-5bc935e25900