United States · FDA National Drug Code directory
Suboxone
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 12496-1208_ad5a289a-6285-4b2d-b7ad-e4812169dd58
- Product NDC
- 12496-1208
- Form
- FILM, SOLUBLE
- Composition / generic term
- buprenorphine hydrochloride, naloxone hydrochloride
- Labeler
- INDIVIOR INC.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20100913
- Source listing expiry
- 20271231
Source-listed ingredients
- BUPRENORPHINE HYDROCHLORIDE — 8 mg/1
- NALOXONE HYDROCHLORIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (12496-1208-3) / 1 FILM, SOLUBLE in 1 POUCH (12496-1208-1) · 12496-1208-3
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →