Active Ingredient: PREDNISOLONE
Proprietary Name: PREDNISOLONE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 5MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: A080354
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: WATSON LABORATORIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information
