Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 10% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 10GM/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016696
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BAXTER HEALTHCARE CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
