FDA
approval
· 2020-12-04
FDA Approved: JANUVIA — Supplemental Application (Merck Sharp & Dohme LLC)
Summary
The FDA approved a supplemental application for Januvia (sitagliptin) from Merck Sharp & Dohme LLC, to the existing NDA for the product.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for JANUVIA (SITAGLIPTIN)