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Dexmedetomidine Hydrochloride in 0.9% Sodium Chloride

NDC 25021-615, dexmedetomidine hydrochloride, injection, solution, from Sagent Pharmaceuticals.

Product NDC
25021-615
Status
Listed
Labeler
Sagent Pharmaceuticals
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA217308
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/25021-615 \
  -H "Authorization: Bearer $HDEV_API_KEY"

Product

Active ingredients and packages

Active ingredients

  • DEXMEDETOMIDINE HYDROCHLORIDE4 ug/mL

Pharmacologic classes

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

Package NDCNDC-11Package
25021-615-502502106155010 BOTTLE in 1 CARTON (25021-615-50) / 50 mL in 1 BOTTLE
25021-615-512502106155110 BOTTLE in 1 CARTON (25021-615-51) / 100 mL in 1 BOTTLE

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/a99335d0-1e87-4180-bde3-cbb12bf91a52

Use it

Look up 25021-615 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/25021-615 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 25021-615. 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.