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
12496-1212_ad5a289a-6285-4b2d-b7ad-e4812169dd58
Product NDC
12496-1212
Form
FILM, SOLUBLE
Composition / generic term
buprenorphine hydrochloride, naloxone hydrochloride
Labeler
INDIVIOR INC.
Marketing category
NDA
Marketing start / end (source format)
20120824
Source listing expiry
20271231

Source-listed ingredients

  • BUPRENORPHINE HYDROCHLORIDE — 12 mg/1
  • NALOXONE HYDROCHLORIDE — 3 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 POUCH in 1 CARTON (12496-1212-3) / 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1) · 12496-1212-3

Source and coverage

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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.

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