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Naloxone Hydrochloride

NDC 70385-2033, Naloxone Hydrochloride, injection, solution, from Sina Health Inc.

Product NDC
70385-2033
Status
Listed
Labeler
Sina Health Inc
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA207633
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70385-2033 \
  -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
70385-2033-1703852033011 VIAL in 1 PACKAGE (70385-2033-1) / 1 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/2879294f-9af9-459e-e063-6394a90a0820

Use it

Look up 70385-2033 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70385-2033 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70385-2033. 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.