Active Ingredient: MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; POTASSIUM PHOSPHATE, MONOBASIC; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM GLUCONATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
Proprietary Name: ISOLYTE S PH 7.4 IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 30MG/100ML;37MG/100ML;0.82MG/100ML;370MG/100ML;530MG/100ML;500MG/100ML;12MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019006
Product Number: 001
Approval Date: Apr 4, 1984
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
