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Naloxone Hydrochloride

NDC 51316-210, Naloxone Hydrochloride, spray, from CVS Pharmacy, Inc.

Product NDC
51316-210
Status
Listed
Labeler
CVS Pharmacy, Inc
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/51316-210 \
  -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
51316-210-02513160210022 VIAL in 1 CARTON (51316-210-02) / .1 mL in 1 VIAL (51316-210-01)

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 51316-210 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/51316-210 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 51316-210. 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.