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Naloxone Hydrochloride

NDC 70069-072, Naloxone Hydrochloride, injection, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-072
Status
Listed
Labeler
Somerset Therapeutics, LLC
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/70069-072 \
  -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
70069-072-107006900721010 CARTON in 1 BOX (70069-072-10) / 1 VIAL, GLASS in 1 CARTON (70069-072-01) / 10 mL in 1 VIAL, GLASS

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/b59ee3cc-9604-4abc-81be-897e2f42aa67

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=70069-072

Use it

Look up 70069-072 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-072 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-072. 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.