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Dexmedetomidine Hydrochloride

NDC 57664-596, DEXMEDETOMIDINE HYDROCHLORIDE, injection, solution, from Sun Pharmaceuticals Industries, Inc..

Product NDC
57664-596
Status
Listed
Labeler
Sun Pharmaceuticals Industries, Inc.
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA202126
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/57664-596 \
  -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
57664-596-505766405965025 VIAL, SINGLE-DOSE in 1 CARTON (57664-596-50) / 2 mL in 1 VIAL, SINGLE-DOSE (57664-596-40)

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4fe788bc-4ad1-4b32-83d3-dcbfcd8429aa

Use it

Look up 57664-596 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/57664-596 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 57664-596. 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.