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NALOXONE HYDROCHLORIDE

NDC 72162-2376, naloxone hydrochloride, spray, from Bryant Ranch Prepack.

Product NDC
72162-2376
Status
Listed
Labeler
Bryant Ranch Prepack
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/72162-2376 \
  -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
72162-2376-2721622376022 VIAL, SINGLE-DOSE in 1 CARTON (72162-2376-2) / .1 mL in 1 VIAL, SINGLE-DOSE (72162-2376-4)

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 72162-2376 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/72162-2376 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 72162-2376. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.

Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.