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NALOXONE HYDROCHLORIDE

NDC 51662-1690, NALOXONE HYDROCHLORIDE, injection, from HF Acquisition Co LLC, DBA HealthFirst.

Product NDC
51662-1690
Status
Listed
Labeler
HF Acquisition Co LLC, DBA HealthFirst
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA213209
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1690 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXONE HYDROCHLORIDE1 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
51662-1690-35166216900310 POUCH in 1 CASE (51662-1690-3) / 1 BOX in 1 POUCH (51662-1690-2) / 1 SYRINGE in 1 BOX (51662-1690-1) / 2 mL in 1 SYRINGE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/53ed164c-dd09-4ea4-e063-6294a90a2434

Use it

Look up 51662-1690 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51662-1690 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51662-1690. 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.