# Zubsolv

NDC: 82111-202
Generic name: buprenorphine hydrochloride and naloxone hydrochloride
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, ORALLY DISINTEGRATING
Routes: SUBLINGUAL
Marketing started: 20260612

FDA application: NDA204242

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: 1.4 mg/1
- NALOXONE HYDROCHLORIDE: .36 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82111-202"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82111-202
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57583c1d-9c44-4503-917d-68dba7377bd1