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Dexmedetomidine Hydrochloride

NDC 70069-758, Dexmedetomidine Hydrochloride, injection, solution, from Somerset Therapeutics, LLC.

Product NDC
70069-758
Status
Listed
Labeler
Somerset Therapeutics, LLC
Dosage form
INJECTION, SOLUTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA218112
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70069-758 \
  -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
70069-758-04700690758044 VIAL in 1 CARTON (70069-758-04) / 4 mL in 1 VIAL

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/649e777b-9b30-4f1e-9fb9-6bba57580976

Use it

Look up 70069-758 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70069-758 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70069-758. 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.