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NALTREXONE HYDROCHLORIDE

NDC 0615-8579, NALTREXONE HYDROCHLORIDE, tablet, film coated, from NCS HealthCare of KY, LLC dba Vangard Labs.

Product NDC
0615-8579
Status
Listed
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
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/0615-8579 \
  -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
0615-8579-390061585793930 TABLET, FILM COATED in 1 BLISTER PACK (0615-8579-39)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/fa2f842f-001a-4f1e-8748-c7852579109c

Use it

Look up 0615-8579 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0615-8579 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0615-8579. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.