NDC 0409-1660 – Precedex

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

Human Prescription Drug

Product NDC0409-1660

Product details

Brand name
Precedex
Generic name
Dexmedetomidine Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
NDA · NDA021038
Marketed since
April 8, 2013
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 (3)

Package NDCDescriptionSince
0409-1660-1010 BOTTLE in 1 TRAY (0409-1660-10) / 100 mL in 1 BOTTLE (0409-1660-35)Apr 8, 2013
0409-1660-2010 VIAL in 1 CARTON (0409-1660-20) / 20 mL in 1 VIAL (0409-1660-22)Jan 5, 2015
0409-1660-5020 BOTTLE in 1 TRAY (0409-1660-50) / 50 mL in 1 BOTTLE (0409-1660-55)Apr 8, 2013

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