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Kvk.tech's list of EU CTD Dossiers, Marketing Authorizations, In, Out Licensing Opportunities & Finished Dosage Formulations aggregated by PharmaCompass

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01 1BENZPHETAMINE HYDROCHLORIDE

02 2BETAXOLOL HYDROCHLORIDE

03 2CYCLOBENZAPRINE HYDROCHLORIDE

04 3HYDROXYZINE HYDROCHLORIDE

05 1PHENDIMETRAZINE TARTRATE

06 6PHENTERMINE HYDROCHLORIDE

07 4PROMETHAZINE HYDROCHLORIDE

08 2SODIUM POLYSTYRENE SULFONATE

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PharmaCompass
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01

Brand Name : BENZPHETAMINE HYDROC...

BioProcess International
Not Confirmed
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Brand Name : BENZPHETAMINE HYDROC...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : BENZPHETAMINE HYDROCHLORI...

Dosage Strength : 50MG

Packaging :

Approval Date : 2010-07-20

Application Number : 90968

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : BETAXOLOL HYDROCHLOR...

BioProcess International
Not Confirmed
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Brand Name : BETAXOLOL HYDROCHLOR...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : BETAXOLOL HYDROCHLORIDE

Dosage Strength : 10MG

Packaging :

Approval Date : 2008-06-27

Application Number : 78962

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : BETAXOLOL HYDROCHLOR...

BioProcess International
Not Confirmed
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Brand Name : BETAXOLOL HYDROCHLOR...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : BETAXOLOL HYDROCHLORIDE

Dosage Strength : 20MG

Packaging :

Approval Date : 2008-06-27

Application Number : 78962

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : CYCLOBENZAPRINE HYDR...

BioProcess International
Not Confirmed
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Brand Name : CYCLOBENZAPRINE HYDR...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : CYCLOBENZAPRINE HYDROCHLO...

Dosage Strength : 5MG

Packaging :

Approval Date : 2011-02-28

Application Number : 78048

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : CYCLOBENZAPRINE HYDR...

BioProcess International
Not Confirmed
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Brand Name : CYCLOBENZAPRINE HYDR...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : CYCLOBENZAPRINE HYDROCHLO...

Dosage Strength : 10MG

Packaging :

Approval Date : 2011-02-28

Application Number : 78048

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : HYDROXYZINE HYDROCHL...

BioProcess International
Not Confirmed
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Brand Name : HYDROXYZINE HYDROCHL...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : HYDROXYZINE HYDROCHLORIDE

Dosage Strength : 10MG

Packaging :

Approval Date : 2007-03-20

Application Number : 40786

Regulatory Info : RX

Registration Country : USA

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07

Brand Name : HYDROXYZINE HYDROCHL...

BioProcess International
Not Confirmed
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Brand Name : HYDROXYZINE HYDROCHL...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : HYDROXYZINE HYDROCHLORIDE

Dosage Strength : 25MG

Packaging :

Approval Date : 2007-03-20

Application Number : 40786

Regulatory Info : RX

Registration Country : USA

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08

Brand Name : HYDROXYZINE HYDROCHL...

BioProcess International
Not Confirmed
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Brand Name : HYDROXYZINE HYDROCHL...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : HYDROXYZINE HYDROCHLORIDE

Dosage Strength : 50MG

Packaging :

Approval Date : 2007-03-20

Application Number : 40786

Regulatory Info : RX

Registration Country : USA

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09

Brand Name : PHENDIMETRAZINE TART...

BioProcess International
Not Confirmed
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Brand Name : PHENDIMETRAZINE TART...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : PHENDIMETRAZINE TARTRATE

Dosage Strength : 35MG

Packaging :

Approval Date : 2010-08-31

Application Number : 91042

Regulatory Info : RX

Registration Country : USA

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10

Brand Name : PHENTERMINE HYDROCHL...

BioProcess International
Not Confirmed
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Brand Name : PHENTERMINE HYDROCHL...

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BioProcess International
Not Confirmed

KVK.Tech

Dosage Form : TABLET;ORAL

Brand Name : PHENTERMINE HYDROCHLORIDE

Dosage Strength : 8MG

Packaging :

Approval Date : 2017-03-17

Application Number : 203436

Regulatory Info : RX

Registration Country : USA

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