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01 1Orion Corporation

02 1AOP Health

03 3Accord healthcare

04 2Actavis Inc

05 1Aristo Pharma GmbH

06 1Aurobindo Pharma Limited

07 1Aurovitas Spain, Sau

08 1Avansor Pharma Oy

09 2Barr Laboratories

10 3Bluefish Pharmaceuticals AB

11 2Chartwell Pharmaceuticals llc

12 2Cipla

13 1Farmatek

14 1GSK

15 1Glenmark Pharmaceuticals

16 2Impax Laboratories

17 1Key Oncologics

18 2Novitium Pharma LLC

19 1ORIFARM GROUP AS

20 2OrPha Swiss

21 2Pharmascience Inc.

22 1Pharmavic Iberica Sl

23 2ROXANE

24 2Rising Pharmaceuticals Inc

25 1SHIRE PLC

26 2STADA Arzneimittel

27 3Sandoz B2B

28 9Takeda Pharmaceutical

29 3Teva Pharmaceutical Industries

30 5Torrent Pharmaceuticals Limited

31 1Urquima S.A. Grupo Uriach

32 1Uxa Farma Sa

33 1V.J. SALOMONE PHARMA LIMITED

34 6Viatris

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PharmaCompass

01

Anagrelide Hydrochloride Monohydrate

Brand Name : Anagrelid Orion

Dosage Form : Capsule

Dosage Strength : 0.5mg

Packaging :

Approval Date : 07/02/2019

Application Number : 20180309000155

Regulatory Info : Approved

Registration Country : Sweden

Fermion Orion Company Banner

02

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76417

Regulatory Info : DISCN

Registration Country : USA

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03

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76417

Regulatory Info : DISCN

Registration Country : USA

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04

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76530

Regulatory Info : DISCN

Registration Country : USA

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05

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76530

Regulatory Info : DISCN

Registration Country : USA

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06

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76683

Regulatory Info : DISCN

Registration Country : USA

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07

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76683

Regulatory Info : DISCN

Registration Country : USA

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08

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76468

Regulatory Info : RX

Registration Country : USA

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09

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76468

Regulatory Info : RX

Registration Country : USA

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10

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76910

Regulatory Info : RX

Registration Country : USA

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11

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76910

Regulatory Info : RX

Registration Country : USA

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12

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76811

Regulatory Info : RX

Registration Country : USA

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13

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76811

Regulatory Info : RX

Registration Country : USA

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14

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2006-06-27

Application Number : 77613

Regulatory Info : DISCN

Registration Country : USA

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15

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2006-06-27

Application Number : 77613

Regulatory Info : DISCN

Registration Country : USA

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16

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76489

Regulatory Info : DISCN

Registration Country : USA

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17

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2005-04-18

Application Number : 76489

Regulatory Info : DISCN

Registration Country : USA

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18

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : AGRYLIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 1997-03-14

Application Number : 20333

Regulatory Info : RX

Registration Country : USA

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19

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : AGRYLIN

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Packaging :

Approval Date : 1997-03-14

Application Number : 20333

Regulatory Info : DISCN

Registration Country : USA

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20

IPPE
Not Confirmed
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IPPE
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 0.5MG BASE

Packaging :

Approval Date : 2017-06-30

Application Number : 209151

Regulatory Info : RX

Registration Country : USA

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