NDC 0338-9555 – Dexmedetomidine Hydrochloride

Dexmedetomidine Hydrochloride 200 ug/50mL · Injection · Intravenous

Human Prescription Drug

Product NDC0338-9555

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride
Labeler
Baxter Healthcare Company
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA208532
Marketed since
August 21, 2018
Listing expires
December 31, 2027
Pharmacologic class
Central alpha-2 Adrenergic Agonist

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0338-9555-2424 BAG in 1 CARTON (0338-9555-24) / 50 mL in 1 BAGAug 21, 2018

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