Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: PREDNISOLONE SODIUM PHOSPHATE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 5MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A075183
Product Number: 001
Approval Date: Mar 26, 2003
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
