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BUPRENORPHINE AND NALOXONE

NDC 0904-7009, buprenorphine and naloxone, tablet, from Major Pharmaceuticals.

Product NDC
0904-7009
Status
Listed
Labeler
Major Pharmaceuticals
Dosage form
TABLET
Route
SUBLINGUAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA203326
DEA schedule
CIII
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7009 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

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

Pharmacologic classes

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

Package NDCNDC-11Package
0904-7009-060090470090650 BLISTER PACK in 1 CARTON (0904-7009-06) / 1 TABLET in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/c5fbec69-e7de-44a8-b9fa-0378ae61a9fe

  • NADAC price for package 00904700906

    GET /v1/drugs/nadac/00904700906

Use it

Look up 0904-7009 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7009 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-7009. 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.