Sodium Acetate 00641-6261-01

Package NDC

00641-6261-01

Manufacturer: Hikma Pharmaceuticals Usa Inc.
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 20, 2024
Listing Expires: December 31, 2026
Application: ANDA216920

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Active Ingredients

Ingredient	Strength
Sodium Acetate Anhydrous	164 mg/mL

Drug Class

Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]

Selected Package

00641-6261-01Selected

1 VIAL in 1 CARTON (0641-6261-01) / 20 mL in 1 VIAL