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NALTREXONE HYDROCHLORIDE

NDC 70518-2718, NALTREXONE HYDROCHLORIDE, tablet, film coated, from REMEDYREPACK INC..

Product NDC
70518-2718
Status
Listed
Labeler
REMEDYREPACK 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/70518-2718 \
  -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
70518-2718-07051827180030 TABLET, FILM COATED in 1 BLISTER PACK (70518-2718-0)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/f821dd49-3fa7-4d33-99de-19023ff1ae65

Use it

Look up 70518-2718 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2718 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2718. 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.