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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 LABS

10 2Bluefish Pharmaceuticals AB

11 2Chartwell Pharmaceuticals llc

12 2Cipla

13 1Farm Agon

14 1Farmatek

15 1GSK

16 1Glenmark Pharmaceuticals

17 2Impax Laboratories

18 1Key Oncologics

19 2Novitium Pharma LLC

20 1ORIFARM GROUP AS

21 2OrPha Swiss

22 2Pharmascience Inc.

23 1Pharmavic Iberica Sl

24 2ROXANE

25 2Rising Pharmaceuticals Inc

26 2SHIRE PLC

27 2STADA Arzneimittel

28 2Sandoz B2B

29 7Takeda Pharmaceutical

30 3Teva Pharmaceutical Industries

31 4Torrent Pharmaceuticals Limited

32 1Urquima S.A. Grupo Uriach

33 1Uxa Farma Sa

34 3Viatris

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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

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

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

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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05

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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06

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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07

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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08

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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09

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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10

Organic Process R&D
Not Confirmed
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Organic Process R&D
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 : DISCN

Registration Country : USA

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11

Organic Process R&D
Not Confirmed
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Organic Process R&D
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 : DISCN

Registration Country : USA

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12

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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13

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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14

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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15

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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16

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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17

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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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18

Organic Process R&D
Not Confirmed
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Organic Process R&D
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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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19

BARR LABS

Country
Organic Process R&D
Not Confirmed
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BARR LABS

Country
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Organic Process R&D
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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20

BARR LABS

Country
Organic Process R&D
Not Confirmed
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BARR LABS

Country
arrow
Organic Process R&D
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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