Active Ingredient: PREDNISOLONE
Proprietary Name: DELTA-CORTEF
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N009987
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PHARMACIA AND UPJOHN CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
