NDC 68083-238 – Dexmedetomidine Hydrochloride

Dexmedetomidine Hydrochloride 4 ug/mL · Injection · Intravenous

Human Prescription Drug

Product NDC68083-238

Product details

Brand name
Dexmedetomidine Hydrochloride
Generic name
Dexmedetomidine Hydrochloride
Labeler
Gland Pharma Limited
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA209307
Marketed since
June 3, 2020
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
68083-238-2020 VIAL in 1 CARTON (68083-238-20) / 50 mL in 1 VIALJun 3, 2020

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