Active Ingredient: DEXTROSE; SODIUM CHLORIDE
Proprietary Name: DEXTROSE 5% AND SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5GM/100ML;900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019483
Product Number: 001
Approval Date: Oct 4, 1985
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status:
Discontinued
Patent and Exclusivity Information
