Potassium Chloride 00409-6651-06

Package NDC

00409-6651-06

Manufacturer: Hospira, Inc.
Dosage Form: Injection, Solution, Concentrate
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: November 10, 2005
Listing Expires: December 31, 2027
Application: ANDA080205

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Active Ingredients

Ingredient	Strength
Potassium Chloride	149 mg/mL

Drug Class

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

Selected Package

00409-6651-06Selected

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6651-06) / 10 mL in 1 VIAL, SINGLE-DOSE (0409-6651-19)