Source: European Medicines Agency (EU) Revision Year: 2020 Publisher: Janssen-Cilag International NV, Turnhoutseweg 30, B-2340, Beerse, Belgium
Erleada 60 mg film-coated tablets.
Pharmaceutical Form |
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Film-coated tablet (tablet). Slightly yellowish to greyish green, oblong-shaped, film-coated tablets (16.7 mm long x 8.7 mm wide), debossed with “AR 60” on one side. |
Each film-coated tablet contains 60 mg of apalutamide.
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Apalutamide |
Apalutamide is an orally administered, selective Androgen Receptor (AR) inhibitor that binds directly to the ligand-binding domain of the AR. Apalutamide treatment decreases tumor cell proliferation and increases apoptosis leading to potent antitumor activity. |
List of Excipients |
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Tablet core: Colloidal anhydrous silica Film-coating: Iron oxide black (E172) |
White opaque high-density polyethylene (HDPE) bottle with a polypropylene (PP) child-resistant closure. Each bottle contains 120 film-coated tablets and a total of 6 g of silica gel desiccant.
PVC-PCTFE foil blister with an aluminum push-through foil sealed inside a wallet pack.
Not all pack sizes may be marketed.
Janssen-Cilag International NV, Turnhoutseweg 30, B-2340, Beerse, Belgium
EU/1/18/1342/001
EU/1/18/1342/002
EU/1/18/1342/003
Date of first authorisation: 14 January 2019
Drug | Countries | |
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ERLEADA | Austria, Brazil, Canada, Cyprus, Ecuador, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Israel, Japan, Lithuania, Netherlands, Poland, Romania, Singapore, Turkey, United Kingdom, United States |
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