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NALTREXONE HYDROCHLORIDE

NDC 0904-7036, NALTREXONE HYDROCHLORIDE, tablet, film coated, from Major Pharmaceuticals.

Product NDC
0904-7036
Status
Listed
Labeler
Major Pharmaceuticals
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA090356
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7036 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALTREXONE HYDROCHLORIDE50 mg/1

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
0904-7036-040090470360430 BLISTER PACK in 1 CARTON (0904-7036-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/69cb8573-08c1-4957-a768-6cd383f6a3f4

  • NADAC price for package 00904703604

    GET /v1/drugs/nadac/00904703604

Use it

Look up 0904-7036 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0904-7036 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0904-7036. 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.