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FDA approval · 2019-04-11

FDA Approved: SANDOSTATIN — Supplemental Application (Novartis Pharmaceuticals Corporation)

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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

  • Sandostatin (Octreotide acetate)

Snippet

SUPPL AP for SANDOSTATIN (OCTREOTIDE ACETATE)