NDC 70121-1712 – Dexmedetomidine Hydrochloride

Dexmedetomidine Hydrochloride 4 ug/mL · Injection · Intravenous

Human Prescription Drug

Product NDC70121-1712

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride in Sodium Chloride
Labeler
Amneal Pharmaceuticals LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA216604
Marketed since
May 19, 2023
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 (2)

Package NDCDescriptionSince
70121-1712-210 POUCH in 1 CARTON (70121-1712-2) / 1 BAG in 1 POUCH / 100 mL in 1 BAGJan 8, 2024
70121-1712-312 POUCH in 1 CARTON (70121-1712-3) / 1 BAG in 1 POUCH / 100 mL in 1 BAGMay 19, 2023

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