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List of All Manufacturers & Suppliers of Methylphenidate Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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01 2Aspen Pharmacare Holdings

02 1Cohance Lifesciences

03 32care4

04 5AFT Pharmaceuticals

05 1Acino Pharma (Pty) Ltd

06 3Actavis Inc

07 4Arrotex Pharmaceuticals

08 4CHEMO

09 4DelNova Healthcare

10 4Janssen-Cilag

11 8Johnson & Johnson Innovative Medicine

12 5MEDICE ARZNEIMITT.PUETTER GmbH

13 11Medice Arzneimittel Pütter GmbH & Co KG

14 3Neos Therapeutics

15 7Novartis Pharmaceuticals Australia Pty Limited

16 5Novartis South Africa (Pty) Ltd

17 4Noven Pharmaceuticals

18 3ORIFARM GROUP AS

19 6SHIRE PLC

20 4Sandoz B2B

21 4Teva Pharma Australia

22 4Teva Pharmaceutical Industries

23 4Viatris

24 20Blank

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Pharmaconex 2024
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Methylphenidate

Brand Name : Adaphen Xl

Dosage Form : SRT

Dosage Strength : 20mg

Packaging : 30X1mg

Approval Date :

Application Number :

Regulatory Info : Originator

Registration Country : South Africa

Aspen API Comapny Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothCohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.

Regulatory Info :

Registration Country : India

Methylphenidate

Brand Name :

Dosage Form : Extended Release Pellet

Dosage Strength : 11%

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : India

Cohance

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Pharmaconex 2024
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Methylphenidate

Brand Name : Adaphen

Dosage Form : TAB

Dosage Strength : 10mg

Packaging : 30X1mg

Approval Date :

Application Number :

Regulatory Info : Generic

Registration Country : South Africa

Aspen API Comapny Banner

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Pharmaconex 2024
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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 8.6MG

Packaging :

Approval Date : 2020-06-19

Application Number : 210924

Regulatory Info : DISCN

Registration Country : USA

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Pharmaconex 2024
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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 17.3MG

Packaging :

Approval Date : 2020-06-19

Application Number : 210924

Regulatory Info : DISCN

Registration Country : USA

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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 25.9MG

Packaging :

Approval Date : 2020-06-19

Application Number : 210924

Regulatory Info : DISCN

Registration Country : USA

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METHYLPHENIDATE

Brand Name : COTEMPLA XR-ODT

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 8.6MG

Packaging :

Approval Date : 2017-06-19

Application Number : 205489

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : COTEMPLA XR-ODT

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 17.3MG

Packaging :

Approval Date : 2017-06-19

Application Number : 205489

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : COTEMPLA XR-ODT

Dosage Form : TABLET, ORALLY DISINTEGRATING, EXTENDED RELEASE;ORAL

Dosage Strength : 25.9MG

Packaging :

Approval Date : 2017-06-19

Application Number : 205489

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : DAYTRANA

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 10MG/9HR (1.1MG/HR)

Packaging :

Approval Date : 2006-04-06

Application Number : 21514

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : DAYTRANA

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 15MG/9HR (1.6MG/HR)

Packaging :

Approval Date : 2006-04-06

Application Number : 21514

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : DAYTRANA

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 20MG/9HR (2.2MG/HR)

Packaging :

Approval Date : 2006-04-06

Application Number : 21514

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : DAYTRANA

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 30MG/9HR (3.3MG/HR)

Packaging :

Approval Date : 2006-04-06

Application Number : 21514

Regulatory Info : RX

Registration Country : USA

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Methylphenidate

Brand Name : Equasym

Dosage Form : Methylphenidate 20Mg 30 Joined' Oral Use Rm

Dosage Strength : 30 cps 20 mg modified release

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 10MG/9HR (1.1MG/HR)

Packaging :

Approval Date : 2022-03-14

Application Number : 206497

Regulatory Info : RX

Registration Country : USA

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Pharmaconex 2024
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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 15MG/9HR (1.6MG/HR)

Packaging :

Approval Date : 2022-03-14

Application Number : 206497

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 20MG/9HR (2.2MG/HR)

Packaging :

Approval Date : 2022-03-14

Application Number : 206497

Regulatory Info : RX

Registration Country : USA

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METHYLPHENIDATE

Brand Name : METHYLPHENIDATE

Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL

Dosage Strength : 30MG/9HR (3.3MG/HR)

Packaging :

Approval Date : 2022-03-14

Application Number : 206497

Regulatory Info : RX

Registration Country : USA

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MEDICE ARZNEIMITT.PUETTER GmbH

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MEDICE ARZNEIMITT.PUETTER GmbH

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Methylphenidate

Brand Name : Medikinet

Dosage Form : Methylphenidate 20Mg 30 Joined' Oral Use Rm

Dosage Strength : 30 cps 20 mg modified release

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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MEDICE ARZNEIMITT.PUETTER GmbH

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Pharmaconex 2024
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MEDICE ARZNEIMITT.PUETTER GmbH

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Pharmaconex 2024
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Methylphenidate

Brand Name : Medikinet

Dosage Form : Methylphenidate 30Mg 30 Joined' Oral Use Rm

Dosage Strength : 30 cps 30 mg modified release

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : Italy

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