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Naloxone Hydrochloride

NDC 70518-2725, Naloxone Hydrochloride, injection, from REMEDYREPACK INC..

Product NDC
70518-2725
Status
Listed
Labeler
REMEDYREPACK INC.
Dosage form
INJECTION
Route
PARENTERAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA072076
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2725 \
  -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
70518-2725-07051827250010 SYRINGE in 1 BOX (70518-2725-0) / 2 mL in 1 SYRINGE (70518-2725-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/68df290c-d776-4cfc-9565-332eb56c4723

Use it

Look up 70518-2725 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70518-2725 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70518-2725. 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.