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Naltrexone Hydrochloride

NDC 63629-1047, Naltrexone Hydrochloride, tablet, film coated, from Bryant Ranch Prepack.

Product NDC
63629-1047
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/63629-1047 \
  -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
63629-1047-163629104701100 TABLET, FILM COATED in 1 BOTTLE (63629-1047-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b773726e-1dc9-415a-81f3-32b43b61b9b1

Use it

Look up 63629-1047 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/63629-1047 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 63629-1047. 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.