Active Ingredient: PREDNISOLONE
Proprietary Name: PRELONE
Dosage Form; Route of Administration: SYRUP; ORAL
Strength: 15MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A089081
Product Number: 001
Approval Date: Feb 4, 1986
Applicant Holder Full Name: TEVA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information