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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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PharmaCompass

01

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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02

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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03

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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04

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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05

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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06

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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07

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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08

Organic Process R&D
Not Confirmed
arrow
arrow
Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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09

Organic Process R&D
Not Confirmed
arrow
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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10

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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11

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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12

Organic Process R&D
Not Confirmed
arrow
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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13

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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14

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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15

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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16

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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17

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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18

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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19

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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20

Organic Process R&D
Not Confirmed
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Organic Process R&D
Not Confirmed

SOTALOL HYDROCHLORIDE

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

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