Active Ingredient: SODIUM CHLORIDE
Proprietary Name: SODIUM CHLORIDE 0.9%
Dosage Form; Route of Administration: SOLUTION; INJECTION
Strength: 90MG/10ML (9MG/ML)
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A201850
Product Number: 001
Approval Date: Jan 20, 2012
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information