01 22care4 ApS
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 5Bristol Myers Squibb
14 1Cheplapharm Arzneimittel Gmbh
15 3Epic Pharma. LLC.
16 4Impax Laboratories
17 11Legacy Pharma
18 4Mepha Pharma
19 4NATCO PHARMA USA
20 4Oxford Pharm
21 4Pharmascience Inc.
22 4Rising Pharmaceuticals Inc
23 6Sandoz B2B
24 7Sun Pharmaceutical Industries Limited
25 9Teva Pharmaceutical Industries
26 4Upsher-Smith Laboratories
27 11Viatris
01 3Antic-calc Tablet
02 1INJ
03 1SOLUTION;INTRAVENOUS
04 1SOLUTION;ORAL
05 1Sotalol 160Mg 50 Combined Oral Use
06 5Sotalol 80Mg 40 Combined Oral Use
07 2Sotalol 80Mg 50 Combined Oral Use
08 4TAB
09 12TABLET
10 72TABLET;ORAL
11 3Tabl
12 1Tablet
13 6Tablets
14 10tablet
01 34DISCN
02 2Generic
03 3Originator
04 6Prescription
05 40RX
06 37Blank
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 1SOTALOLO TEVA
16 1SOTYLIZE
17 2Solavert
18 6Sotacor
19 1Sotahexal 160
20 1Sotahexal 80
21 1Sotalex
22 5Sotalol
23 2Sotalol 2care4
24 6Sotalol Mylan
25 2Sotalol Sandoz
26 4Sotalol-Mepha
01 10Australia
02 6Canada
03 14Italy
04 3Norway
05 5South Africa
06 6Sweden
07 4Switzerland
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 : 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
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
LOOKING FOR A SUPPLIER?