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

View source ↗

Summary

The FDA approved a supplemental application for PROMACTA (eltrombopag olamine) submitted by Novartis Pharmaceuticals Corporation.

Upgrade for the full analysis, importance score, and drug timeline.

Diseases / indications

• Aplastic Anemia
• Immune Thrombocytopenia

Drugs mentioned

• Promacta (eltrombopag)

Snippet

SUPPL AP for PROMACTA (ELTROMBOPAG OLAMINE)