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01 2Zenara Pharma

02 2Alkem Laboratories

03 2Amdipharm Mercury Company Limited

04 2Annora Pharma

05 4Apotex Inc

06 2Appco Pharmaceutical Corp

07 2Assia Chemical Industries Ltd

08 2H2-PHARMA

09 2Hikma Pharmaceuticals

10 2JAMP PHARMA

11 2Kolmar Korea Co., Ltd.

12 2Laboratorio Eczane Pharma

13 2Lupin Ltd

14 2MSN Laboratories

15 2Mallinckrodt Pharmaceuticals

16 2Mirpharm

17 2Nora Pharma

18 2Novitium Pharma LLC

19 2Razi Al Madina Pharmaceuticals

20 6SHIRE PLC

21 2SKG-Pharma

22 2Somerset Pharmaceuticals Inc

23 4Takeda Pharmaceutical

24 2Torrent Pharmaceuticals Limited

25 2Zydus Pharmaceuticals

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PharmaCompass

01

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218795

Regulatory Info : RX

Registration Country : USA

Biophore CB

02

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218795

Regulatory Info : RX

Registration Country : USA

Biophore CB

03

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218295

Regulatory Info : RX

Registration Country : USA

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04

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218295

Regulatory Info : RX

Registration Country : USA

blank

05

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 217662

Regulatory Info : RX

Registration Country : USA

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06

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 217662

Regulatory Info : RX

Registration Country : USA

blank

07

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218847

Regulatory Info : RX

Registration Country : USA

blank

08

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218847

Regulatory Info : RX

Registration Country : USA

blank

09

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218177

Regulatory Info : RX

Registration Country : USA

blank

10

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218177

Regulatory Info : RX

Registration Country : USA

blank

11

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2024-12-26

Application Number : 218492

Regulatory Info : RX

Registration Country : USA

blank

12

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2024-12-26

Application Number : 218492

Regulatory Info : RX

Registration Country : USA

blank

13

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218812

Regulatory Info : RX

Registration Country : USA

blank

14

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218812

Regulatory Info : RX

Registration Country : USA

blank

15

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : MOTEGRITY

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2018-12-14

Application Number : 210166

Regulatory Info : RX

Registration Country : USA

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16

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : MOTEGRITY

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2018-12-14

Application Number : 210166

Regulatory Info : RX

Registration Country : USA

blank

17

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218778

Regulatory Info : DISCN

Registration Country : USA

blank

18

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-06-24

Application Number : 218778

Regulatory Info : DISCN

Registration Country : USA

blank

19

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2025-08-07

Application Number : 218056

Regulatory Info : RX

Registration Country : USA

blank

20

FNCE
Not Confirmed
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FNCE
Not Confirmed

PRUCALOPRIDE SUCCINATE

Brand Name : PRUCALOPRIDE SUCCINATE

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 2MG BASE

Packaging :

Approval Date : 2025-08-07

Application Number : 218056

Regulatory Info : RX

Registration Country : USA

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