Active Ingredient: CALCIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM CHLORIDE; SODIUM LACTATE
Proprietary Name: LACTATED RINGER'S IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 20MG/100ML;30MG/100ML;600MG/100ML;310MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N017641
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ICU MEDICAL INC
Marketing Status:
Prescription
Patent and Exclusivity Information
