01 2AAIPharma Services Corp.
02 2ANDA Repository
03 1Acino Pharma (Pty) Ltd
04 2Actavis Inc
05 2Amneal Pharmaceuticals
06 2Bausch Health
07 2Carnegie Pharmaceuticals
08 1Curatis
09 1FHTA
10 2Grupo Chemo
11 2Hikma Pharmaceuticals
12 2Impax Laboratories
13 2Lannett Company, Inc.
14 1Link Healthcare
15 2Oxford Pharm
16 3Rubicon Research
17 1SIT LABORATORIO FARMAC. Srl
18 2XYZ Pharma
01 1Primidone 250Mg 30 Joined' Oral Use
02 1SUSPENSION
03 1SUSPENSION;ORAL
04 1TAB
05 3TABLET
06 23TABLET;ORAL
07 1Tabl
08 1tablet
01 8DISCN
02 2Generics
03 1Originator
04 2Prescription
05 16RX
06 3Blank
01 3MYSOLINE
02 4Mysoline
03 23PRIMIDONE
04 2primidone CHEMO®
01 1Australia
02 2Canada
03 2Costa Rica
04 1Italy
05 1South Africa
06 1Switzerland
07 24USA
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PRIMIDONE
Dosage Form : TABLET
Dosage Strength : 250MG
Packaging : 100/500
Approval Date :
Application Number : 396761
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : Prescription
Registration Country : Canada
Brand Name : PRIMIDONE
Dosage Form : TABLET
Dosage Strength : 125MG
Packaging : 100/500
Approval Date :
Application Number : 399310
Regulatory Info : Prescription
Registration Country : Canada
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 1982-01-01
Application Number : 83551
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 1982-01-01
Application Number : 85052
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-04-23
Application Number : 40866
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2008-04-23
Application Number : 40866
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2005-09-29
Application Number : 40626
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2005-09-29
Application Number : 40626
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYSOLINE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 1982-01-01
Application Number : 9170
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MYSOLINE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 1982-01-01
Application Number : 9170
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2024-01-23
Application Number : 218366
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2024-01-23
Application Number : 218366
Regulatory Info : RX
Registration Country : USA
Regulatory Info :
Registration Country : Switzerland
Brand Name : Mysoline
Dosage Form : Tabl
Dosage Strength : 250mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Switzerland
Regulatory Info : Generics
Registration Country : Costa Rica
Brand Name : primidone CHEMO®
Dosage Form : TABLET
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generics
Registration Country : Costa Rica
Regulatory Info : Generics
Registration Country : Costa Rica
Brand Name : primidone CHEMO®
Dosage Form : SUSPENSION
Dosage Strength : 250MG/5ML
Packaging :
Approval Date :
Application Number :
Regulatory Info : Generics
Registration Country : Costa Rica
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2006-07-27
Application Number : 40667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2006-07-27
Application Number : 40667
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-02-12
Application Number : 40717
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2008-02-12
Application Number : 40717
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 1982-01-01
Application Number : 84903
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2001-05-24
Application Number : 84903
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2005-02-24
Application Number : 40586
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2005-02-24
Application Number : 40586
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2022-06-28
Application Number : 214896
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2022-06-28
Application Number : 214896
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 125MG
Packaging :
Approval Date : 2022-12-28
Application Number : 214896
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 50MG
Packaging :
Approval Date : 2008-10-03
Application Number : 40862
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PRIMIDONE
Dosage Form : TABLET;ORAL
Dosage Strength : 250MG
Packaging :
Approval Date : 2008-10-03
Application Number : 40862
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MYSOLINE
Dosage Form : SUSPENSION;ORAL
Dosage Strength : 250MG/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 10401
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info :
Registration Country : Italy
Brand Name : Mysoline
Dosage Form : Primidone 250Mg 30 Joined' Oral Use
Dosage Strength : 30 CPR 250 mg
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Italy
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
LOOKING FOR A SUPPLIER?