Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 3% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 3GM/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A209476
Product Number: 001
Approval Date: Mar 13, 2019
Applicant Holder Full Name: FRESENIUS KABI USA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
