NDC 0409-1174 – Precedex

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

Human Prescription Drug

Product NDC0409-1174

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 7, 2022
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
0409-1174-1010 BOTTLE in 1 TRAY (0409-1174-10) / 100 mL in 1 BOTTLE (0409-1174-01)Mar 7, 2022

Other Precedex products