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

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01 5FCT
02 58Film Coated Tablet
03 3Film-Coated Tablet
04 42TABLET
05 104TABLET;ORAL
06 5Tablet
07 14tablet
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01 2APO-Lurasidone
02 5AURO-LURASIDONE
03 5JAMP LURASIDONE
04 9LATUDA
05 4LURASIDONE
06 99LURASIDONE HYDROCHLORIDE
07 2LURASIDONE SUN
08 2LURASIDONE-WGR
09 23Latuda
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21 5Lurobran
22 1MAKTUDA 120 mg
23 1MAKTUDA 20 mg
24 1MAKTUDA 40 mg
25 1MAKTUDA 60 mg
26 1MAKTUDA 80 mg
27 4NRA-LURASIDONE
28 5PMS-LURASIDONE
29 2Pharmacor Lurasidone
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11 104USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : RX
Registration Country : USA
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
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
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
European CDMO and Gx manufacturer with 75 years of experience in delivering premium APIs to pharmaceutical partners worldwide.
Regulatory Info : Approved
Registration Country : Sweden
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
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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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

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Regulatory Info : RX
Registration Country : USA
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

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Regulatory Info :
Registration Country : USA
Brand Name : LURASIDONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 20MG
Packaging :
Approval Date :
Application Number : 207948
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : LURASIDONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number : 207948
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : LURASIDONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 60MG
Packaging :
Approval Date :
Application Number : 207948
Regulatory Info :
Registration Country : USA

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Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info :
Registration Country : USA
Brand Name : LURASIDONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 80MG
Packaging :
Approval Date :
Application Number : 207948
Regulatory Info :
Registration Country : USA

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Regulatory Info :
Registration Country : USA
Brand Name : LURASIDONE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 120MG
Packaging :
Approval Date :
Application Number : 207948
Regulatory Info :
Registration Country : USA

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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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

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Regulatory Info : RX
Registration Country : USA
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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Regulatory Info : RX
Registration Country : USA
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

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
Regulatory Info : RX
Registration Country : USA
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
