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Naltrexone Hydrochloride

NDC 72162-2529, Naltrexone Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
72162-2529
Status
Listed
Labeler
Bryant Ranch Prepack
Dosage form
TABLET, FILM COATED
Route
ORAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA075274
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2529 \
  -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
72162-2529-172162252901100 TABLET, FILM COATED in 1 BOTTLE (72162-2529-1)
72162-2529-37216225290330 TABLET, FILM COATED in 1 BOTTLE (72162-2529-3)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/637ed3da-476d-4f95-8bbc-f93eaa0aa57e

Use it

Look up 72162-2529 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2529 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2529. 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.