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Naloxone Hydrochloride

NDC 0641-6205, Naloxone Hydrochloride, injection, from Hikma Pharmaceuticals USA Inc..

Product NDC
0641-6205
Status
Listed
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
INJECTION
Route
INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA212300
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6205 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • NALOXONE HYDROCHLORIDE1 mg/mL

Pharmacologic classes

Opioid Antagonist [EPC]; Opioid Antagonists [MoA]

Package NDCNDC-11Package
0641-6205-100064162051010 SYRINGE in 1 CARTON (0641-6205-10) / 2 mL in 1 SYRINGE (0641-6205-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/e6467385-6990-498c-8a0e-f4a40ef33cb7

  • Medicare Part B payment limits (ASP)

    GET /v1/drugs/asp?ndc=0641-6205

  • NADAC price for package 00641620510

    GET /v1/drugs/nadac/00641620510

Use it

Look up 0641-6205 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/0641-6205 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 0641-6205. 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.