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01 4Dr. Reddy's Laboratories

02 3Polpharma

03 32care4

04 11Accord healthcare

05 5Actavis Inc

06 5Alembic Pharmaceuticals Limited

07 5Alkem Laboratories

08 2Alphapharm PTY Ltd

09 5Amneal Pharmaceuticals

10 15Angelini Pharma

11 5Annora Pharma

12 2Apotex Inc

13 5Auro Pharma Inc

14 5Aurobindo Pharma Limited

15 5Avet Pharmaceuticals

16 5Chartwell Pharmaceuticals llc

17 3Cinfa

18 5Exeltis

19 3G.L. Pharma Gmbh

20 2Generic Health

21 3Genericon Pharma Ges.M.B.H.

22 5InvaGen Pharmaceuticals Inc

23 5JAMP PHARMA

24 5Jubilant Generics

25 3Laboratorios Liconsa

26 5Lupin Ltd

27 5MSN Laboratories

28 10Macleods Pharmaceuticals Limited

29 4Medius Ag

30 4Nora Pharma

31 4ORIFARM GROUP AS

32 5Orchid Pharma

33 5Par Pharmaceutical

34 2Pharmacore Inc

35 5Pharmascience Inc.

36 4SANIS HEALTH INC

37 7Sandoz B2B

38 4Sumitomo Pharma

39 7Sun Pharmaceutical Industries Limited

40 5Sunovion Pharmaceuticals

41 5Taro Pharmaceutical Industries

42 6Tecnimede

43 8Teva Pharmaceutical Industries

44 5Torrent Pharmaceuticals Limited

45 5Unichem Laboratories Limited

46 2WAGNER PHARMACEUTICALS PTY LTD

47 5Zydus Pharmaceuticals

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2021-08-24

Application Number : 208047

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Regulatory Info : Approved

Registration Country : Sweden

Lurasidonhydroklorid

Brand Name : Polur

Dosage Form : Film Coated Tablet

Dosage Strength : 18.5mg

Packaging :

Approval Date : 14/05/2025

Application Number : 20240923000013

Regulatory Info : Approved

Registration Country : Sweden

Polpharma CB

03

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2021-08-24

Application Number : 208047

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

04

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 2021-08-24

Application Number : 208047

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

05

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

Regulatory Info : RX

Registration Country : USA

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG

Packaging :

Approval Date : 2021-08-24

Application Number : 208047

Regulatory Info : RX

Registration Country : USA

Dr Reddy Company Banner

06

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Regulatory Info : Approved

Registration Country : Sweden

Lurasidonhydroklorid

Brand Name : Polur

Dosage Form : Film Coated Tablet

Dosage Strength : 37mg

Packaging :

Approval Date : 14/05/2025

Application Number : 20240923000020

Regulatory Info : Approved

Registration Country : Sweden

Polpharma CB

07

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothEuropean CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.

Regulatory Info : Approved

Registration Country : Sweden

Lurasidonhydroklorid

Brand Name : Polur

Dosage Form : Film Coated Tablet

Dosage Strength : 74mg

Packaging :

Approval Date : 14/05/2025

Application Number : 20240923000037

Regulatory Info : Approved

Registration Country : Sweden

Polpharma CB

08

Pharmapack
Not Confirmed
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2019-01-03

Application Number : 208002

Regulatory Info : RX

Registration Country : USA

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09

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2019-01-03

Application Number : 208002

Regulatory Info : RX

Registration Country : USA

blank

10

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 2019-01-03

Application Number : 208002

Regulatory Info : RX

Registration Country : USA

blank

11

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date :

Application Number : 207948

Regulatory Info :

Registration Country : USA

blank

12

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date :

Application Number : 207948

Regulatory Info :

Registration Country : USA

blank

13

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date :

Application Number : 207948

Regulatory Info :

Registration Country : USA

blank

14

Pharmapack
Not Confirmed
arrow
arrow
Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG

Packaging :

Approval Date :

Application Number : 207948

Regulatory Info :

Registration Country : USA

blank

15

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LURASIDONE HYDROCHLORIDE

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Packaging :

Approval Date :

Application Number : 207948

Regulatory Info :

Registration Country : USA

blank

16

Pharmapack
Not Confirmed
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LATUDA

Dosage Form : TABLET;ORAL

Dosage Strength : 40MG

Packaging :

Approval Date : 2010-10-28

Application Number : 200603

Regulatory Info : RX

Registration Country : USA

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17

Pharmapack
Not Confirmed
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LATUDA

Dosage Form : TABLET;ORAL

Dosage Strength : 80MG

Packaging :

Approval Date : 2010-10-28

Application Number : 200603

Regulatory Info : RX

Registration Country : USA

blank

18

Pharmapack
Not Confirmed
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LATUDA

Dosage Form : TABLET;ORAL

Dosage Strength : 20MG

Packaging :

Approval Date : 2011-12-07

Application Number : 200603

Regulatory Info : RX

Registration Country : USA

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19

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LATUDA

Dosage Form : TABLET;ORAL

Dosage Strength : 120MG

Packaging :

Approval Date : 2012-04-26

Application Number : 200603

Regulatory Info : RX

Registration Country : USA

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20

Pharmapack
Not Confirmed
arrow
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Pharmapack
Not Confirmed

LURASIDONE HYDROCHLORIDE

Brand Name : LATUDA

Dosage Form : TABLET;ORAL

Dosage Strength : 60MG

Packaging :

Approval Date : 2013-07-12

Application Number : 200603

Regulatory Info : RX

Registration Country : USA

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