NDC 0409-1638 – Precedex

Dexmedetomidine Hydrochloride 100 ug/mL · Injection, Solution, Concentrate · Intravenous

Human Prescription Drug

Product NDC0409-1638

Product details

Brand name
Precedex
Generic name
Dexmedetomidine Hydrochloride
Labeler
Hospira, Inc.
Dosage form
Injection, Solution, Concentrate
Route
Intravenous
Marketing category
NDA · NDA021038
Marketed since
November 30, 2004
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
0409-1638-0225 VIAL in 1 TRAY (0409-1638-02) / 2 mL in 1 VIAL (0409-1638-32)Nov 30, 2004

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