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Naltrexone Hydrochloride

NDC 64850-300, Naltrexone Hydrochloride, tablet, film coated, from Elite Laboratories, Inc..

Product NDC
64850-300
Status
Listed
Labeler
Elite Laboratories, Inc.
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/64850-300 \
  -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
64850-300-0164850030001100 TABLET, FILM COATED in 1 BOTTLE (64850-300-01)
64850-300-306485003003030 TABLET, FILM COATED in 1 BOTTLE (64850-300-30)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/5f188bdc-2009-43aa-ad32-f06dbfac2642

  • NADAC price for package 64850030001

    GET /v1/drugs/nadac/64850030001

  • NADAC price for package 64850030030

    GET /v1/drugs/nadac/64850030030

Use it

Look up 64850-300 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/64850-300 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 64850-300. 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.