# Suboxone

NDC: 12496-1208
Generic name: buprenorphine hydrochloride, naloxone hydrochloride
Labeler / Manufacturer: INDIVIOR INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: FILM, SOLUBLE
Routes: BUCCAL, SUBLINGUAL
Marketing started: 20100913

FDA application: NDA022410

## Active ingredients

- BUPRENORPHINE HYDROCHLORIDE: 8 mg/1
- NALOXONE HYDROCHLORIDE: 2 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"12496-1208"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=12496-1208
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8a5edcf9-828c-4f97-b671-268ab13a8ecd