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FDA approval · 2018-06-06

FDA Approved: PRED FORTE — Supplemental Application (Allergan, Inc.)

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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

  • PRED FORTE (Prednisolone acetate)

Snippet

SUPPL AP for PRED FORTE (PREDNISOLONE ACETATE)