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NALTREXONE HYDROCHLORIDE

NDC 47335-326, NALTREXONE HYDROCHLORIDE, tablet, film coated, from Sun Pharmaceutical Industries, Inc..

Product NDC
47335-326
Status
Listed
Labeler
Sun Pharmaceutical Industries, Inc.
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/47335-326 \
  -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
47335-326-0847335032608100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08)
47335-326-18473350326181000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18)
47335-326-834733503268330 TABLET, FILM COATED in 1 BOTTLE (47335-326-83)
47335-326-8847335032688100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/0f30f885-d0cd-4fa6-a8e0-142f08a56792

  • NADAC price for package 47335032683

    GET /v1/drugs/nadac/47335032683

  • NADAC price for package 47335032688

    GET /v1/drugs/nadac/47335032688

Use it

Look up 47335-326 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/47335-326 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 47335-326. 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.