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Dexmedetomidine Hydrochloride

NDC 70121-1712, Dexmedetomidine Hydrochloride in Sodium Chloride, injection, from Amneal Pharmaceuticals LLC.

Product NDC
70121-1712
Status
Listed
Labeler
Amneal Pharmaceuticals LLC
Dosage form
INJECTION
Route
INTRAVENOUS
Product type
HUMAN PRESCRIPTION DRUG
Marketing category
ANDA
Application
ANDA216604
DEA schedule
None
Request
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1712 \
  -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
70121-1712-27012117120210 POUCH in 1 CARTON (70121-1712-2) / 1 BAG in 1 POUCH / 100 mL in 1 BAG
70121-1712-37012117120312 POUCH in 1 CARTON (70121-1712-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAG

Linked data

RxNorm, label and prices

RxNorm concepts

Related lookups

  • FDA label sections

    GET /v1/drugs/labels/4df8cc35-fc80-4438-b982-9c4b7d17bad2

Use it

Look up 70121-1712 from code or an agent

curl
curl https://api.healthcare.dev/v1/drugs/ndc/70121-1712 \
  -H "Authorization: Bearer $HDEV_API_KEY"
MCP prompt
Using the healthcare.dev MCP server, look up NDC 70121-1712. 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.