Active Ingredient: CALCIUM CHLORIDE; DEXTROSE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN DEXTROSE 5% AND LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;5GM/100ML;179MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A211428
Product Number: 001
Approval Date: Nov 9, 2021
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
