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NALOXONE HYDROCHLORIDE

NDC 71205-707, naloxone hydrochloride, spray, from Proficient Rx LP.

Product NDC
71205-707
Status
Listed
Labeler
Proficient Rx LP
Dosage form
SPRAY
Route
NASAL
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA211951
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/71205-707 \
  -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
71205-707-02712050707022 VIAL, SINGLE-DOSE in 1 CARTON (71205-707-02) / .1 mL in 1 VIAL, SINGLE-DOSE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/8d529b4c-85fd-4e50-9443-9080825307bf

Use it

Look up 71205-707 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/71205-707 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 71205-707. 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.