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01 1Accord healthcare

02 2Actavis Inc

03 2BARR LABS

04 2Chartwell Pharmaceuticals llc

05 2Esjay Pharma

06 1Farm Agon

07 1Farmatek

08 2IVAX Pharmaceuticals Inc

09 2Impax Laboratories

10 1Key Oncologics

11 4Nordic Pharma

12 1ORIFARM GROUP AS

13 3OrPha Swiss

14 2Pharmascience Inc.

15 2ROXANE

16 2Rising Pharmaceuticals Inc

17 3SHIRE PLC

18 1Sandoz B2B

19 5Takeda Pharmaceutical

20 1Teva Pharmaceutical Industries

21 4Torrent Pharmaceuticals Limited

22 1Viatris

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PharmaCompass

01

RDD 2025
Not Confirmed
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RDD 2025
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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02

RDD 2025
Not Confirmed
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RDD 2025
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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03

RDD 2025
Not Confirmed
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RDD 2025
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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04

RDD 2025
Not Confirmed
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RDD 2025
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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05

RDD 2025
Not Confirmed
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RDD 2025
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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06

RDD 2025
Not Confirmed
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RDD 2025
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

blank

07

RDD 2025
Not Confirmed
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RDD 2025
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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08

RDD 2025
Not Confirmed
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RDD 2025
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

blank

09

RDD 2025
Not Confirmed
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RDD 2025
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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10

RDD 2025
Not Confirmed
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RDD 2025
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

blank

11

RDD 2025
Not Confirmed
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RDD 2025
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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12

RDD 2025
Not Confirmed
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RDD 2025
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

blank

13

RDD 2025
Not Confirmed
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RDD 2025
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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14

RDD 2025
Not Confirmed
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RDD 2025
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

blank

15

RDD 2025
Not Confirmed
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RDD 2025
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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16

RDD 2025
Not Confirmed
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RDD 2025
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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17

RDD 2025
Not Confirmed
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RDD 2025
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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18

RDD 2025
Not Confirmed
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RDD 2025
Not Confirmed

ANAGRELIDE HYDROCHLORIDE

Brand Name : ANAGRELIDE HYDROCHLORIDE

Dosage Form : CAPSULE;ORAL

Dosage Strength : EQ 1MG BASE

Packaging :

Approval Date : 2017-06-30

Application Number : 209151

Regulatory Info : RX

Registration Country : USA

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19

BARR LABS

Country
RDD 2025
Not Confirmed
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BARR LABS

Country
arrow
RDD 2025
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
RDD 2025
Not Confirmed
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BARR LABS

Country
arrow
RDD 2025
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

blank