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NALOXONE HYDROCHLORIDE

NDC 80425-0409, naloxone hydrochloride, spray, from Advanced Rx of Tennessee, LLC.

Product NDC
80425-0409
Status
Listed
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
SPRAY
Route
NASAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA211951
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0409 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXONE HYDROCHLORIDE4 mg/.1mL

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
80425-0409-1804250409012 VIAL, SINGLE-DOSE in 1 CARTON (80425-0409-1) / .1 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

No FDA label, Medicare Part B payment limit or NADAC price is linked to this product.

Use it

Look up 80425-0409 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/80425-0409 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 80425-0409. 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.