Active Ingredient: PREDNISOLONE ACETATE
Proprietary Name: PREDNISOLONE ACETATE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 25MG/ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084717
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: CENTRAL PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information