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NALOXONE HYDROCHLORIDE

NDC 51662-1673, NALOXONE HYDROCHLORIDE, injection, solution, from HF Acquisition Co. LLC. DBA HealthFirst.

Product NDC
51662-1673
Status
Listed
Labeler
HF Acquisition Co. LLC. DBA HealthFirst
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207634
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1673 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXONE HYDROCHLORIDE.4 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
51662-1673-15166216730110 mL in 1 VIAL, GLASS (51662-1673-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4d66b96a-acbb-2292-e063-6294a90af788

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=51662-1673

Use it

Look up 51662-1673 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1673 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1673. 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.