# Zubsolv

NDC: 54123-907
Generic name: buprenorphine hydrochloride and naloxone hydrochloride
Labeler / Manufacturer: Orexo US, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: SUBLINGUAL
Marketing started: 20130704

FDA application: NDA204242

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: .7 mg/1
- NALOXONE HYDROCHLORIDE: .18 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54123-907"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54123-907
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5f5cfcfe-d52b-49e6-8fe4-550477332dd2