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01 22care4
02 1ANGENERICO SpA
03 4Actavis Inc
04 4AiPing Pharmaceutical Inc
05 2Alphapharm PTY Ltd
06 1AltaThera
07 11Apotex Inc
08 4Arrow Pharmaceuticals
09 3Aurobindo Pharma Limited
10 1Azurity Pharma
11 2BGP Group of Companies
12 6Beximco Pharmaceuticals
13 4Bristol Myers Squibb
14 2Bristol-Myers Squibb Ab
15 2Cheplapharm Arzneimittel Gmbh
16 1Ebb Medical
17 3Epic Pharma. LLC.
18 4Esjay Pharma
19 4Impax Laboratories
20 11Legacy Pharma
21 2Mepha Pharma
22 2ORIFARM GROUP AS
23 4Oxford Pharm
24 4Pharmascience Inc.
25 2Ratiopharm GmbH
26 4Rising Pharmaceuticals Inc
27 6Sandoz B2B
28 7Sun Pharmaceutical Industries Limited
29 9Teva Pharmaceutical Industries
30 4Upsher-Smith Laboratories
31 11Viatris
32 2WAGNER PHARMACEUTICALS PTY LTD
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01 3Antic-calc Tablet
02 1INJ
03 1Injectable Solution
04 1SOLUTION;INTRAVENOUS
05 1SOLUTION;ORAL
06 1Sotalol 160Mg 50 Combined Oral Use
07 5Sotalol 80Mg 40 Combined Oral Use
08 2Sotalol 80Mg 50 Combined Oral Use
09 4TAB
10 6TABLET
11 72TABLET;ORAL
12 14Tablet
13 6Tablets
14 12tablet
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01 2Allowed
02 3Approved
03 34DISCN
04 10Deregistered
05 2Generic
06 3Originator
07 2Prescription
08 40RX
09 33Blank
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01 2APO-SOTALOL
02 2APX-Sotalol
03 5BETAPACE
04 6BETAPACE AF
05 2Cardol
06 2PMS-SOTALOL - 160 MG
07 2PMS-SOTALOL - 80 MG
08 1RYTMOBETA
09 2Rytmobeta
10 4SORINE
11 1SOTALEX
12 1SOTALOL
13 58SOTALOL HYDROCHLORIDE
14 2SOTALOL MYLAN GENERICS
15 2SOTALOL-WGR
16 1SOTALOLO TEVA
17 1SOTYLIZE
18 2Solavert
19 8Sotacor
20 1Sotahexal 160
21 1Sotahexal 80
22 1Sotalex
23 5Sotalol
24 2Sotalol 2Care4
25 1Sotalol Ebb
26 4Sotalol Mylan
27 2Sotalol Orifarm
28 2Sotalol Ratiopharm
29 2Sotalol Sandoz
30 2Sotalol Viatris
31 2Sotalol-Mepha
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01 12Australia
02 6Canada
03 14Italy
04 3Norway
05 5South Africa
06 13Sweden
07 2Switzerland
08 74USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 80MG
Packaging :
Approval Date : 2000-07-13
Application Number : 75238
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2000-07-13
Application Number : 75238
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 160MG
Packaging :
Approval Date : 2000-07-13
Application Number : 75238
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 240MG
Packaging :
Approval Date : 2000-07-13
Application Number : 75238
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : SOLUTION;INTRAVENOUS
Dosage Strength : 150MG/10ML (15MG/ML)
Packaging :
Approval Date : 2009-07-02
Application Number : 22306
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 80MG
Packaging :
Approval Date : 2000-05-01
Application Number : 75237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2000-05-01
Application Number : 75237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 160MG
Packaging :
Approval Date : 2000-05-01
Application Number : 75237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOTALOL HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 240MG
Packaging :
Approval Date : 2000-05-01
Application Number : 75237
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE
Dosage Form : TABLET;ORAL
Dosage Strength : 80MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE
Dosage Form : TABLET;ORAL
Dosage Strength : 160MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE
Dosage Form : TABLET;ORAL
Dosage Strength : 240MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAPACE
Dosage Form : TABLET;ORAL
Dosage Strength : 320MG
Packaging :
Approval Date : 1992-10-30
Application Number : 19865
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 1994-04-20
Application Number : 19865
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 80MG
Packaging :
Approval Date : 2000-02-22
Application Number : 21151
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date : 2000-02-22
Application Number : 21151
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 160MG
Packaging :
Approval Date : 2000-02-22
Application Number : 21151
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 100MG
Packaging :
Approval Date : 2003-03-14
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 40MG
Packaging :
Approval Date : 2003-04-02
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : BETAPACE AF
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date : 2003-04-02
Application Number : 21151
Regulatory Info : DISCN
Registration Country : USA