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Picato (ingenol mebutate)

Additional monitoring
Region
🇪🇺 EU
Active substance
ingenol mebutate
Company
LEO Laboratories Ltd.
Status
Withdrawn
Therapeutic area
Keratosis, Actinic
EU approval
Thu 15 Nov 2012
Designations
Additional monitoring
Application
EMEA/H/C/002275
ATC
D06BX02
Official record
www.ema.europa.eu

Indication

Picato is indicated for the cutaneous treatment of non?hyperkeratotic, non?hypertrophic actinic keratosis in adults.

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.