NDC 0409-7838 – Precedex

Dexmedetomidine Hydrochloride 4 ug/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC0409-7838

Product details

Brand name
Precedex
Generic name
Dexmedetomidine Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA021038
Marketed since
March 24, 2025
Listing expires
December 31, 2027
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Precedex →

Package NDC codes (1)

Package NDCDescriptionSince
0409-7838-2424 POUCH in 1 CASE (0409-7838-24) / 1 BAG in 1 POUCH / 50 mL in 1 BAG (0409-7838-01)Mar 24, 2025

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