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Naltrexone Hydrochloride

NDC 71335-3011, Naltrexone Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
71335-3011
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/71335-3011 \
  -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
71335-3011-17133530110130 TABLET, FILM COATED in 1 BOTTLE (71335-3011-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8f019ac1-13a8-42f2-bdb2-8aaef5896d96

Use it

Look up 71335-3011 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71335-3011 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71335-3011. 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.