Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9%
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 180MG/20ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A217535
Product Number: 002
Approval Date: Aug 23, 2023
Applicant Holder Full Name: NEXUS PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information
