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Suboxone

NDC 12496-1212, buprenorphine hydrochloride, naloxone hydrochloride, film, soluble, from INDIVIOR INC..

Product NDC
12496-1212
Status
Listed
Labeler
INDIVIOR INC.
Dosage form
FILM, SOLUBLE
Route
BUCCAL, SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA022410
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/12496-1212 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • BUPRENORPHINE HYDROCHLORIDE12 mg/1
  • NALOXONE HYDROCHLORIDE3 mg/1

Pharmacologic classes

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

Package NDCNDC-11Package
12496-1212-31249612120330 POUCH in 1 CARTON (12496-1212-3) / 1 FILM, SOLUBLE in 1 POUCH (12496-1212-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8a5edcf9-828c-4f97-b671-268ab13a8ecd

  • NADAC price for package 12496121203

    GET /v1/drugs/nadac/12496121203

Use it

Look up 12496-1212 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/12496-1212 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 12496-1212. 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.