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Dexmedetomidine Hydrochloride

NDC 65219-642, dexmedetomidine hydrochloride, injection, solution, from Fresenius Kabi USA, LLC.

Product NDC
65219-642
Status
Listed
Labeler
Fresenius Kabi USA, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA201072
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/65219-642 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMEDETOMIDINE HYDROCHLORIDE100 ug/mL

Pharmacologic classes

Adrenergic alpha2-Agonists [MoA]; Central alpha-2 Adrenergic Agonist [EPC]; General Anesthesia [PE]

Package NDCNDC-11Package
65219-642-026521906420225 VIAL in 1 TRAY (65219-642-02) / 2 mL in 1 VIAL (65219-642-01)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/1896a96e-25f8-494e-9a96-6463b52fb102

Use it

Look up 65219-642 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/65219-642 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 65219-642. 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.