FDA
approval
· 2018-06-06
FDA Approved: PRED FORTE — Supplemental Application (Allergan, Inc.)
Summary
The FDA approved a supplemental application for PRED FORTE (prednisolone acetate ophthalmic suspension) submitted by Allergan, Inc.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for PRED FORTE (PREDNISOLONE ACETATE)