FDA
approval
· 2019-04-11
FDA Approved: SANDOSTATIN — Supplemental Application (Novartis Pharmaceuticals Corporation)
Summary
The FDA approved a supplemental application for Sandostatin (octreotide acetate) from Novartis Pharmaceuticals Corporation under NDA 019667.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for SANDOSTATIN (OCTREOTIDE ACETATE)