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01 8CSL Vifor
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01 4POWDER;ORAL
02 4Powder For Oral Suspension
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01 4Approved
02 1DISCN
03 3RX
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01 4VELTASSA
02 4Veltassa
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01 4Sweden
02 4USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VELTASSA
Dosage Form : POWDER;ORAL
Dosage Strength : EQ 8.4GM BASE/PACKET
Packaging :
Approval Date : 2015-10-21
Application Number : 205739
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VELTASSA
Dosage Form : POWDER;ORAL
Dosage Strength : EQ 16.8GM BASE/PACKET
Packaging :
Approval Date : 2015-10-21
Application Number : 205739
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : VELTASSA
Dosage Form : POWDER;ORAL
Dosage Strength : EQ 25.2GM BASE/PACKET
Packaging :
Approval Date : 2015-10-21
Application Number : 205739
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : VELTASSA
Dosage Form : POWDER;ORAL
Dosage Strength : EQ 1GM BASE/PACKET
Packaging :
Approval Date : 2023-10-02
Application Number : 205739
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Veltassa
Dosage Form : Powder For Oral Suspension
Dosage Strength : 1.0g
Packaging :
Approval Date : 05/01/2024
Application Number : 20221110000078
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Veltassa
Dosage Form : Powder For Oral Suspension
Dosage Strength : 16.8g
Packaging :
Approval Date : 19/07/2017
Application Number : 20160420000029
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Veltassa
Dosage Form : Powder For Oral Suspension
Dosage Strength : 25.2g
Packaging :
Approval Date : 19/07/2017
Application Number : 20160420000036
Regulatory Info : Approved
Registration Country : Sweden
Regulatory Info : Approved
Registration Country : Sweden
Brand Name : Veltassa
Dosage Form : Powder For Oral Suspension
Dosage Strength : 8.4g
Packaging :
Approval Date : 19/07/2017
Application Number : 20160420000012
Regulatory Info : Approved
Registration Country : Sweden