United States · FDA National Drug Code directory

Buprenorphine and Naloxone Sublingual Film

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
67296-1933_46e93923-334d-68db-e063-6394a90ad902
Product NDC
67296-1933
Form
FILM
Composition / generic term
Buprenorphine and Naloxone
Labeler
Redpharm Drug
Marketing category
ANDA
Marketing start / end (source format)
20190211
Source listing expiry
20261231

Source-listed ingredients

  • BUPRENORPHINE HYDROCHLORIDE — 8 mg/1
  • NALOXONE HYDROCHLORIDE DIHYDRATE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 POUCH in 1 CARTON (67296-1933-1) / 1 FILM in 1 POUCH · 67296-1933-1
  • 9 POUCH in 1 CARTON (67296-1933-9) / 1 FILM in 1 POUCH · 67296-1933-9

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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