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List of All Manufacturers & Suppliers of MolPort-001-685-316 Licensing, EU CTD Dossiers, Marketing Authorizations, Finished Dosage Formulations listed on PharmaCompass.com

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$ API Ref.Price (USD/KG) : 161Xls
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01 3Taro Pharmaceutical Industries

02 2Aucta Pharmaceuticals

03 3Breckenridge Pharmaceutical

04 62care4

05 72care4 ApS

06 3ANI Pharmaceuticals Inc

07 3Actavis Inc

08 3Ajanta Pharma Limited

09 1Alkem Laboratories

10 1Amneal Pharmaceuticals

11 3Annora Pharma

12 6Apotex Inc

13 1Biocon

14 3Biofarma Pharmaceutical Industry and Commerce Inc

15 1Bionpharma

16 1Chartwell Pharmaceuticals llc

17 3Desitin Arzneimittel

18 2Ebb Medical AB

19 3Glenmark Pharmaceuticals

20 4Hainan Poly Pharm

21 1Hetero Drugs

22 4Hikma Pharmaceuticals

23 3Jubilant Cadista Pharmaceuticals

24 2Kusum Healthcare Pvt Ltd

25 4Macleods Pharmaceuticals Limited

26 4Medartuum AB

27 1Medley Pharmaceuticals Ltd.

28 7Novartis Pharmaceuticals Australia Pty Limited

29 20Novartis Pharmaceuticals Corporation

30 2Novartis South Africa (Pty) Ltd

31 10ORIFARM GROUP AS

32 4Paranova Group AS

33 3Pharmachim AB

34 1Renew Biopharma

35 7Rubicon Research

36 3STADA Arzneimittel

37 1Smith & Kenner Pharmaceuticals

38 4Sun Pharmaceutical Industries Limited

39 3Supernus Pharmaceuticals

40 2TECNIGEN Srl

41 3TWi Pharmaceuticals

42 6Tecnimede

43 2Torrent Pharmaceuticals Limited

44 3Umedica Laboratories

45 2Xixia Pharmaceuticals (Pty) Ltd

46 3Zydus Lifesciences

47 14Blank

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAucta is a global brand that creates better products from proven molecules.

Regulatory Info : RX

Registration Country : USA

OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 300MG/5ML

Packaging :

Approval Date : 2022-11-30

Application Number : 215332

Regulatory Info : RX

Registration Country : USA

Aucta Company Banner

02

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2008-01-11

Application Number : 78069

Regulatory Info : RX

Registration Country : USA

Breckenridge Pharmaceutical

03

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2007-11-15

Application Number : 77801

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2007-11-15

Application Number : 77801

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2007-11-15

Application Number : 77801

Regulatory Info : RX

Registration Country : USA

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06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothAucta is a global brand that creates better products from proven molecules.

Regulatory Info :

Registration Country : U.S.A

Oxcarbamazepine

Brand Name :

Dosage Form : Oral Suspension

Dosage Strength : 300MG/5ML

Packaging :

Approval Date :

Application Number :

Regulatory Info :

Registration Country : U.S.A

Aucta Company Banner

07

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2008-01-11

Application Number : 78069

Regulatory Info : RX

Registration Country : USA

Breckenridge Pharmaceutical

08

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2008-01-11

Application Number : 78069

Regulatory Info : RX

Registration Country : USA

Breckenridge Pharmaceutical

09

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2007-10-09

Application Number : 77795

Regulatory Info : DISCN

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2007-10-09

Application Number : 77795

Regulatory Info : DISCN

Registration Country : USA

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OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2000-01-14

Application Number : 21014

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2000-01-14

Application Number : 21014

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2000-01-14

Application Number : 21014

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : TRILEPTAL

Dosage Form : SUSPENSION;ORAL

Dosage Strength : 300MG/5ML

Packaging :

Approval Date : 2001-05-25

Application Number : 21285

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2008-04-09

Application Number : 77747

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2008-04-09

Application Number : 77747

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2008-04-09

Application Number : 77747

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 150MG

Packaging :

Approval Date : 2007-10-09

Application Number : 77794

Regulatory Info : RX

Registration Country : USA

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19

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 300MG

Packaging :

Approval Date : 2007-10-09

Application Number : 77794

Regulatory Info : RX

Registration Country : USA

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OXCARBAZEPINE

Brand Name : OXCARBAZEPINE

Dosage Form : TABLET;ORAL

Dosage Strength : 600MG

Packaging :

Approval Date : 2007-10-09

Application Number : 77794

Regulatory Info : RX

Registration Country : USA

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