Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.225% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;225MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N017606
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
