Active Ingredient: SODIUM LACTATE
Proprietary Name: SODIUM LACTATE 1/6 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: N020004
Product Number: 001
Approval Date: Apr 21, 1992
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:
Discontinued
Patent and Exclusivity Information