NDC 63323-421 – Dexmedetomidine Hydrochloride

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

Human Prescription Drug

Product NDC63323-421

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine hydrochloride
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA201072
Marketed since
September 18, 2015
Listing expires
December 31, 2026
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

Uses, dosage, side effects and warnings for Dexmedetomidine Hydrochloride →

Package NDC codes (1)

Package NDCDescriptionSince
63323-421-0225 VIAL in 1 TRAY (63323-421-02) / 2 mL in 1 VIAL (63323-421-01)Sep 18, 2015

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