# IBU

NDC: 55111-682
Generic name: Ibuprofen
Labeler / Manufacturer: Dr. Reddy's Laboratories Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20081120

FDA application: ANDA075682

## Active ingredients

- IBUPROFEN: 400 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55111-682"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55111-682
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=24731405-219c-79b4-ecf0-7d5fbfda94ba