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Naloxone Hydrochloride Injection, USP, Auto-Injector

NDC 60842-002, Naloxone Hydrochloride, injection, solution, from Kaleo, Inc..

Product NDC
60842-002
Status
Listed
Labeler
Kaleo, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
NDA
Application
NDA215457
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/60842-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXONE HYDROCHLORIDE10 mg/.4mL

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
60842-002-026084200020210 DOSE PACK in 1 CARTON (60842-002-02) / .4 mL in 1 DOSE PACK

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b5463553-b775-47a3-8d10-31e01ca1ec72

Use it

Look up 60842-002 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/60842-002 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 60842-002. 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.