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NALTREXONE HYDROCHLORIDE

NDC 71610-919, naltrexone hydrochloride, tablet, film coated, from Aphena Pharma Solutions - Tennessee, LLC.

Product NDC
71610-919
Status
Listed
Labeler
Aphena Pharma Solutions - Tennessee, 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/71610-919 \
  -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
71610-919-3171610091931600 TABLET, FILM COATED in 1 BOTTLE (71610-919-31)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/390bff41-7bab-b72a-e063-6294a90ad35d

Use it

Look up 71610-919 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71610-919 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71610-919. 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.