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01 2Accord healthcare

02 2Amneal Pharmaceuticals

03 2Aurobindo Pharma Limited

04 2Chartwell Pharmaceuticals llc

05 2Cosette Pharma

06 2Daiichi Sankyo Europe GmbH

07 2HEC Pharm

08 1JAMP PHARMA

09 2Lupin Ltd

10 2Panacea Biotec Limited

11 2Senores Pharmaceuticals

12 2Unichem Laboratories Limited

13 2Unichem Pharmaceuticals USA, Inc

14 2Viatris

15 2Zentiva

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PharmaCompass

01

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2018-02-02

Application Number : 205987

Regulatory Info : RX

Registration Country : USA

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02

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2018-02-02

Application Number : 205987

Regulatory Info : RX

Registration Country : USA

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03

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2018-06-19

Application Number : 205913

Regulatory Info : RX

Registration Country : USA

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04

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2018-06-19

Application Number : 205913

Regulatory Info : RX

Registration Country : USA

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05

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205888

Regulatory Info : RX

Registration Country : USA

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06

APS Symposium
Not Confirmed
arrow
arrow
APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205888

Regulatory Info : RX

Registration Country : USA

blank

07

APS Symposium
Not Confirmed
arrow
arrow
APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205790

Regulatory Info : DISCN

Registration Country : USA

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08

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205790

Regulatory Info : DISCN

Registration Country : USA

blank

09

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : EFFIENT

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2009-07-10

Application Number : 22307

Regulatory Info : RX

Registration Country : USA

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10

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : EFFIENT

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2009-07-10

Application Number : 22307

Regulatory Info : RX

Registration Country : USA

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11

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2019-01-16

Application Number : 206021

Regulatory Info : RX

Registration Country : USA

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12

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2019-01-16

Application Number : 206021

Regulatory Info : RX

Registration Country : USA

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13

APS Symposium
Not Confirmed
arrow
arrow
APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2023-01-09

Application Number : 205930

Regulatory Info : DISCN

Registration Country : USA

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14

APS Symposium
Not Confirmed
arrow
arrow
APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2023-01-09

Application Number : 205930

Regulatory Info : DISCN

Registration Country : USA

blank

15

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205897

Regulatory Info : RX

Registration Country : USA

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16

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2017-10-16

Application Number : 205897

Regulatory Info : RX

Registration Country : USA

blank

17

APS Symposium
Not Confirmed
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2020-07-07

Application Number : 205926

Regulatory Info : DISCN

Registration Country : USA

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18

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2020-07-07

Application Number : 205926

Regulatory Info : DISCN

Registration Country : USA

blank

19

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 5MG BASE

Packaging :

Approval Date : 2017-07-12

Application Number : 205927

Regulatory Info : RX

Registration Country : USA

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20

APS Symposium
Not Confirmed
arrow
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APS Symposium
Not Confirmed

PRASUGREL HYDROCHLORIDE

Brand Name : PRASUGREL

Dosage Form : TABLET;ORAL

Dosage Strength : EQ 10MG BASE

Packaging :

Approval Date : 2017-07-12

Application Number : 205927

Regulatory Info : RX

Registration Country : USA

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