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NALTREXONE HYDROCHLORIDE

NDC 0406-1170, naltrexone hydrochloride, tablet, film coated, from SpecGx LLC.

Product NDC
0406-1170
Status
Listed
Labeler
SpecGx LLC
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/0406-1170 \
  -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
0406-1170-0100406117001100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01)
0406-1170-030040611700330 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/06ff2d5a-e62b-4fa4-bbdb-01938535bc65

  • NADAC price for package 00406117001

    GET /v1/drugs/nadac/00406117001

  • NADAC price for package 00406117003

    GET /v1/drugs/nadac/00406117003

Use it

Look up 0406-1170 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0406-1170 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0406-1170. 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.