Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 450MG/50ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: A211968
Product Number: 001
Approval Date: Apr 23, 2020
Applicant Holder Full Name: NEPHRON PHARMACEUTICALS CORPORATION
Marketing Status:
Prescription
Patent and Exclusivity Information