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: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N019480
Product Number: 001
Approval Date: Sep 17, 1985
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
