Active Ingredient: SODIUM LACTATE
Proprietary Name: SODIUM LACTATE 0.167 MOLAR IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 1.87GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N016692
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
