01 1Accord healthcare
02 2Actavis Inc
03 2Barr Laboratories
04 2Chartwell Pharmaceuticals llc
05 1Farm Agon
06 1Farmatek
07 2IVAX Pharmaceuticals Inc
08 2Impax Laboratories
09 1Key Oncologics
10 2NATCO PHARMA USA
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
01 1Anagrelide 0.5Mg 100 Unita' Oral Use
02 2CAP
03 3CAPSULE
04 20CAPSULE;ORAL
05 1Caps
06 2Capsule
07 3Capsule, hard
08 1HARD CAPSULES
09 1Hard Capsule
10 1Hard Capsule For Oral Use
11 3Hard Capsules
12 3Kaps
13 4Tabl
01 13DISCN
02 2Generic
03 1Originator
04 2Prescription
05 7RX
06 20Blank
01 2AGRYLIN
02 1ANAGRELIDE ACCORD
03 18ANAGRELIDE HYDROCHLORIDE
04 1ANAGRELIDE SANDZ
05 1ANAGRELIDE TEVA
06 1ANAGRELIDE VIATRIS
07 1Agrylin 0,5 mg
08 3Anagrelid Nordic
09 1Anagrelide Nordic
10 2PMS-ANAGRELIDE
11 3Thromboreductin
12 1Thromboreductin 0.5mg
13 1XAGRID
14 6Xagrid
15 3Blank
01 2Canada
02 1India
03 6Italy
04 3Norway
05 2South Africa
06 1Sweden
07 8Switzerland
08 1Turkey
09 20USA
10 1United Kingdom
Regulatory Info :
Registration Country : Italy
Brand Name : ANAGRELIDE ACCORD
Dosage Form : Hard Capsules
Dosage Strength : 0.5 mg
Packaging : 100 UNITS 0.5 MG - ORAL USE
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info :
Registration Country : Turkey
Brand Name :
Dosage Form : Capsule
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Turkey
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info :
Registration Country : Norway
Brand Name : Xagrid
Dosage Form : Capsule, hard
Dosage Strength : 0.5 mg
Packaging : Bottle of plastic
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PMS-ANAGRELIDE
Dosage Form : CAPSULE
Dosage Strength : 0.5MG
Packaging : 100
Approval Date :
Application Number :
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info :
Registration Country : Sweden
Brand Name : Xagrid
Dosage Form : HARD CAPSULES
Dosage Strength : 0.5 MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Sweden
Regulatory Info :
Registration Country : Italy
Brand Name : Xagrid
Dosage Form : Anagrelide 0.5Mg 100 Unita' Oral Use
Dosage Strength : 100 cps 0.5 mg bottle
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Regulatory Info :
Registration Country : Norway
Brand Name : Xagrid
Dosage Form : Capsule, hard
Dosage Strength : 0.5 mg
Packaging : Bottle
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : DISCN
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : RX
Registration Country : USA
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
Regulatory Info : Generic
Registration Country : United Kingdom
Brand Name :
Dosage Form : CAPSULE
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : United Kingdom
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Capsule
Dosage Strength : 0.5MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
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
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Norway
Brand Name : Xagrid
Dosage Form : Capsule, hard
Dosage Strength : 0.5 mg
Packaging : Bottle of plastic
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Norway
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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