FDA
label_change
· 2016-10-12
FDA Approved: PROMACTA — Supplemental Application (Novartis Pharmaceuticals Corporation)
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
Snippet
SUPPL AP for PROMACTA (ELTROMBOPAG OLAMINE)