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Ximelagatran 36 mg film coated tablets (ximelagatran)

Region
🇪🇺 EU
Active substance
ximelagatran
Company
AstraZeneca
Status
Application withdrawn
Therapeutic area
Atrial Fibrillation
Application
EMEA/H/C/000702
Official record
www.ema.europa.eu

Regulatory milestones

No milestones recorded in the last year.

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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.