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Naloxone Hydrochloride

NDC 69238-2104, Naloxone Hydrochloride, spray, from Amneal Pharmaceuticals LLC.

Product NDC
69238-2104
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
SPRAY
Route
NASAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA217992
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2104 \
  -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
69238-2104-7692382104072 VIAL, SINGLE-DOSE in 1 CARTON (69238-2104-7) / .1 mL in 1 VIAL, SINGLE-DOSE (69238-2104-1)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • NADAC price for package 69238210407

    GET /v1/drugs/nadac/69238210407

Use it

Look up 69238-2104 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/69238-2104 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 69238-2104. 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.