Active Ingredient: PREDNISOLONE ACETATE
Proprietary Name: PRED FORTE
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N017011
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ABBVIE INC
Marketing Status:
Prescription
Patent and Exclusivity Information
