Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 900MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A207956
Product Number: 001
Approval Date: May 25, 2017
Applicant Holder Full Name: LABORATORIOS GRIFOLS SA
Marketing Status:
Prescription
Patent and Exclusivity Information
