Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: PREDNISOLONE SODIUM PHOSPHATE
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: EQ 25MG BASE/5ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AA
Application Number: A091396
Product Number: 001
Approval Date: Sep 13, 2010
Applicant Holder Full Name: MISSION PHARMACAL CO
Marketing Status:
Prescription
Patent and Exclusivity Information
