Source: European Medicines Agency (EU) Revision Year: 2020 Publisher: Otsuka Pharmaceutical Netherlands B.V., Herikerbergweg 292, 1101 CT, Amsterdam, Netherlands
Samsca 7.5 mg tablets.
Samsca 15 mg tablets.
Samsca 30 mg tablets.
Pharmaceutical Form |
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Tablet. Samsca 7.5 mg tablets: Blue, rectangular, shallow-convex tablets with dimensions of 7.7 × 4.35 × 2.5 mm, debossed with “OTSUKA” and “7.5” on one side. Samsca 15 mg tablets: Blue, triangular, shallow-convex tablets with dimensions of 6.58 × 6.2 × 2.7 mm, debossed with “OTSUKA” and “15” on one side. Samsca 30 mg tablets: Blue, round, shallow-convex tablets with dimensions of Ø8 × 3.0 mm, debossed with “OTSUKA” and “30” on one side. |
Samsca 7.5 mg tablets: Each tablet contains 7.5 mg tolvaptan.
Excipient with known effect: 51 mg lactose (as monohydrate) per tablet
Samsca 15 mg tablets: Each tablet contains 15 mg tolvaptan.
Excipient with known effect: 35 mg lactose (as monohydrate) per tablet
Samsca 30 mg tablets: Each tablet contains 30 mg tolvaptan.
Excipient with known effect: 70 mg lactose (as monohydrate) per tablet
For the full list of excipients, see section 6.1.
Active Ingredient | Description | |
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Tolvaptan |
Tolvaptan is a selective vasopressin V2-receptor antagonist that specifically blocks the binding of arginine vasopressin (AVP) at the V2-receptor of the distal portions of the nephron. Tolvaptan affinity for the human V2-receptor is 1.8 times that of native AVP. |
List of Excipients |
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Maize starch |
Samsca 7.5 mg tablets:
10 tablets in PP/Alu blisters
30 tablets in PP/Alu blisters
10 × 1 tablet in PVC/Alu perforated unit dose blisters
30 × 1 tablet in PVC/Alu perforated unit dose blisters
Samsca 15 mg and Samsca 30 mg tablets:
10 × 1 tablet in PVC/Alu perforated unit dose blisters
30 × 1 tablet in PVC/Alu perforated unit dose blisters
Not all pack sizes may be marketed.
Otsuka Pharmaceutical Netherlands B.V., Herikerbergweg 292, 1101 CT, Amsterdam, Netherlands
Samsca 7.5 mg tablets:
EU/1/09/539/005 (10 tablets)
EU/1/09/539/006 (30 tablets)
EU/1/09/539/007 (10 × 1 tablet)
EU/1/09/539/008 (30 × 1 tablet)
Samsca 15 mg tablets:
EU/1/09/539/001 (10 × 1 tablet)
EU/1/09/539/002 (30 × 1 tablet)
Samsca 30 mg tablets:
EU/1/09/539/003 (10 × 1 tablet)
EU/1/09/539/004 (30 × 1 tablet)
Date of first authorisation: 03 August 2009
Date of latest renewal: 19 June 2014
Drug | Countries | |
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SAMSCA | Austria, Canada, Estonia, Spain, Finland, France, Hong Kong, Croatia, Ireland, Italy, Japan, Lithuania, Poland, Romania, Turkey, United Kingdom, United States |
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