# Butrans

NDC: 59011-751
Generic name: buprenorphine
Labeler / Manufacturer: Knoa Pharma LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20110214

FDA application: NDA021306

## Active ingredients

- BUPRENORPHINE: 10 ug/h

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"59011-751"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59011-751
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=794aa355-66de-41b8-aedf-f2c40f6bc664