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:
Application Number: A075099
Product Number: 001
Approval Date: Jun 28, 2002
Applicant Holder Full Name: PHARMOBEDIENT CONSULTING
Marketing Status:
Discontinued
Patent and Exclusivity Information
