FDA Approved: SUSVIMO — Supplemental Application (Genentech, Inc.)

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Summary

The FDA approved a supplemental application for SUSVIMO (ranibizumab) submitted by Genentech, Inc. The action relates to a regulatory update for this product.

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Diseases / indications

• Wet Age-related Macular Degeneration

Drugs mentioned

• SUSVIMO (Ranibizumab)

Snippet

SUPPL AP for SUSVIMO (RANIBIZUMAB)