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FDA label_change · 2016-10-12

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

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Summary

FDA approved a supplemental application for PROMACTA (eltrombopag olamine) to update its labeling; this action may include changes to indications and dosing.

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Diseases / indications

Drugs mentioned

  • Promacta (eltrombopag)

Snippet

SUPPL AP for PROMACTA (ELTROMBOPAG OLAMINE)