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

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01 1ALBUTEROL SULFATE

02 1BRIMONIDINE TARTRATE; TIMOLOL MALEATE

03 1BROMFENAC SODIUM

04 1CIPROFLOXACIN; DEXAMETHASONE

05 1ERYTHROMYCIN

06 1KETOTIFEN FUMARATE

07 1LIDOCAINE HYDROCHLORIDE

08 3LOTEPREDNOL ETABONATE

09 1OFLOXACIN

10 1TIMOLOL MALEATE

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PharmaCompass
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01

Brand Name : ALBUTEROL SULFATE

Discovery on Target
Not Confirmed
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Brand Name : ALBUTEROL SULFATE

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SOLUTION;INHALATION

Brand Name : ALBUTEROL SULFATE

Dosage Strength : EQ 0.5% BASE

Packaging :

Approval Date : 1998-01-15

Application Number : 74543

Regulatory Info : RX

Registration Country : USA

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02

Brand Name : BRIMONIDINE TARTRATE...

Discovery on Target
Not Confirmed
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Brand Name : BRIMONIDINE TARTRATE...

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SOLUTION/DROPS;OPHTHALMI...

Brand Name : BRIMONIDINE TARTRATE AND ...

Dosage Strength : 0.2%;EQ 0.5% BASE

Packaging :

Approval Date : 2022-10-31

Application Number : 91086

Regulatory Info : RX

Registration Country : USA

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03

Brand Name : BROMFENAC SODIUM

Discovery on Target
Not Confirmed
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Brand Name : BROMFENAC SODIUM

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SOLUTION/DROPS;OPHTHALMI...

Brand Name : BROMFENAC SODIUM

Dosage Strength : EQ 0.09% ACID

Packaging :

Approval Date : 2014-01-22

Application Number : 203395

Regulatory Info : RX

Registration Country : USA

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04

Brand Name : CIPROFLOXACIN AND DE...

Luxepack
Not Confirmed
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Brand Name : CIPROFLOXACIN AND DE...

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Luxepack
Not Confirmed

Sentiss Pharma

Dosage Form : SUSPENSION/DROPS;OTIC

Brand Name : CIPROFLOXACIN AND DEXAMET...

Dosage Strength : 0.3%;0.1%

Packaging :

Approval Date : 2023-06-09

Application Number : 215768

Regulatory Info : RX

Registration Country : USA

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05

Brand Name : ERYTHROMYCIN

Discovery on Target
Not Confirmed
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Brand Name : ERYTHROMYCIN

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : OINTMENT;OPHTHALMIC

Brand Name : ERYTHROMYCIN

Dosage Strength : 0.5%

Packaging :

Approval Date : 1996-07-18

Application Number : 64030

Regulatory Info : RX

Registration Country : USA

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06

Brand Name : KETOTIFEN FUMARATE

Discovery on Target
Not Confirmed
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Brand Name : KETOTIFEN FUMARATE

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SOLUTION/DROPS;OPHTHALMI...

Brand Name : KETOTIFEN FUMARATE

Dosage Strength : EQ 0.025% BASE

Packaging :

Approval Date : 2007-07-26

Application Number : 77958

Regulatory Info : OTC

Registration Country : USA

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07

Brand Name : LIDOCAINE HYDROCHLOR...

Discovery on Target
Not Confirmed
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Brand Name : LIDOCAINE HYDROCHLOR...

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : JELLY;TOPICAL

Brand Name : LIDOCAINE HYDROCHLORIDE

Dosage Strength : 2%

Packaging :

Approval Date : 2003-02-12

Application Number : 40433

Regulatory Info : RX

Registration Country : USA

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08

Brand Name : LOTEPREDNOL ETABONAT...

Discovery on Target
Not Confirmed
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Brand Name : LOTEPREDNOL ETABONAT...

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SUSPENSION/DROPS;OPHTHAL...

Brand Name : LOTEPREDNOL ETABONATE

Dosage Strength : 0.5%

Packaging :

Approval Date : 2019-04-17

Application Number : 207609

Regulatory Info : RX

Registration Country : USA

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09

Brand Name : LOTEPREDNOL ETABONAT...

Discovery on Target
Not Confirmed
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Brand Name : LOTEPREDNOL ETABONAT...

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : GEL;OPHTHALMIC

Brand Name : LOTEPREDNOL ETABONATE

Dosage Strength : 0.5%

Packaging :

Approval Date : 2021-02-10

Application Number : 212080

Regulatory Info : RX

Registration Country : USA

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10

Brand Name : LOTEPREDNOL ETABONAT...

Discovery on Target
Not Confirmed
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Brand Name : LOTEPREDNOL ETABONAT...

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Discovery on Target
Not Confirmed

Sentiss Pharma

Dosage Form : SUSPENSION/DROPS;OPHTHAL...

Brand Name : LOTEPREDNOL ETABONATE

Dosage Strength : 0.2%

Packaging :

Approval Date : 2023-04-12

Application Number : 215933

Regulatory Info : RX

Registration Country : USA

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