0781-3494 : Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride In 0.9% Sodium Chloride 4 ug/ml Intravenous Injection


NDC: 0781-3494
Labeler: Sandoz Inc.
Product Type: Human Prescription Drug
Drug Name:  Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride
Dosage Form: Intravenous Injection
Application #: ANDA209065
Rev. Date: 


NDC Package Codes:

  • 0781-3494-95: 10 VIAL IN 1 CARTON (0781‑3494‑95) > 50 ML IN 1 VIAL

Active Ingredients:

  • Dexmedetomidine Hydrochloride

Dosage Strength:

  • 4 ug/mL

Pharmaceutical Classes:

  • Adrenergic alpha2-Agonists [MoA]
  • Central alpha-2 Adrenergic Agonist [EPC]
  • General Anesthesia [PE]

Related Products:

Based on records with the same trade name.
  • 0781-3493 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride In 0.9% Sodium Chloride 4 ug/ml Intravenous Injection by Sandoz Inc.
  • 0781-3495 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride In 0.9% Sodium Chloride 4 ug/ml Intravenous Injection by Sandoz Inc.
  • 43066-555 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride In 0.9% Sodium Chloride 200 ug/50ml Intravenous Injection by Baxter Healthcare Corporation
  • 43066-557 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride In 0.9% Sodium Chloride 400 ug/100ml Intravenous Injection by Baxter Healthcare Corporation

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