Potassium Chloride 51662-1421-01

Package NDC

51662-1421-01

Manufacturer: Hf Acquisition Co Llc, Dba Healthfirst
Dosage Form: Injection, Solution, Concentrate
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 18, 2019
Listing Expires: December 31, 2026
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

51662-1421-01Selected

20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1)