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NALTREXONE HYDROCHLORIDE

NDC 51407-959, naltrexone hydrochloride, tablet, film coated, from Golden State Medical Supply, Inc..

Product NDC
51407-959
Status
Listed
Labeler
Golden State Medical Supply, Inc.
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA076264
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51407-959 \
  -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
51407-959-0151407095901100 TABLET, FILM COATED in 1 BOTTLE (51407-959-01)
51407-959-305140709593030 TABLET, FILM COATED in 1 BOTTLE (51407-959-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/3cbd0cad-7c56-ac0a-e063-6294a90a80e4

Use it

Look up 51407-959 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51407-959 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51407-959. 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.