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Naloxone Hydrochloride

NDC 0591-3871, Naloxone Hydrochloride, spray, metered, from Actavis Pharma, Inc..

Product NDC
0591-3871
Status
Listed
Labeler
Actavis Pharma, Inc.
Dosage form
SPRAY, METERED
Route
NASAL
Product type
HUMAN OTC DRUG
Marketing category
ANDA
Application
ANDA209522
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3871 \
  -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
0591-3871-99005913871992 BLISTER PACK in 1 CARTON (0591-3871-99) / 1 VIAL, SINGLE-DOSE in 1 BLISTER PACK (0591-3871-54) / .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 0591-3871 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0591-3871 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0591-3871. 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.