Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.45% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 450MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AP
Application Number: N019759
Product Number: 001
Approval Date: Jun 8, 1988
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:
Prescription
Patent and Exclusivity Information