Active Ingredient: POTASSIUM CHLORIDE; SODIUM CHLORIDE
Proprietary Name: POTASSIUM CHLORIDE 20MEQ IN SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 149MG/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019686
Product Number: 001
Approval Date: Oct 17, 1988
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information