Active Ingredient: SODIUM LACTATE
Proprietary Name: SODIUM LACTATE IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 5MEQ/ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018947
Product Number: 001
Approval Date: Sep 5, 1984
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
