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Buprenorphine and Naloxone

NDC 67296-2228, buprenorphine and naloxone, film, from Redpharm Drug.

Product NDC
67296-2228
Status
Listed
Labeler
Redpharm Drug
Dosage form
FILM
Route
BUCCAL, SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212756
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2228 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE2 mg/1
  • NALOXONE HYDROCHLORIDE.5 mg/1

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]; Partial Opioid Agonist [EPC]; Partial Opioid Agonists [MoA]

Package NDCNDC-11Package
67296-2228-1672962228016 POUCH in 1 CARTON (67296-2228-1) / 1 FILM in 1 POUCH
67296-2228-36729622280330 POUCH in 1 CARTON (67296-2228-3) / 1 FILM in 1 POUCH

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5005a6c8-9a3b-a99a-e063-6294a90aac13

Use it

Look up 67296-2228 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/67296-2228 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 67296-2228. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
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Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.