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01 4FENOFIBRATE

02 2SOLIFENACIN SUCCINATE

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PharmaCompass

01

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
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Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
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AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : FENOFIBRATE

Dosage Strength : 54MG

Approval Date : 2017-12-19

Application Number : 207803

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : FENOFIBRATE

Dosage Strength : 160MG

Approval Date : 2017-12-19

Application Number : 207803

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : FENOFIBRATE

Dosage Strength : 48MG

Approval Date : 2021-02-10

Application Number : 208476

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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04

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

Brand Name : FENOFIBRATE

BioFlorida Conference
Not Confirmed
arrow

AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : FENOFIBRATE

Dosage Strength : 145MG

Approval Date : 2021-02-10

Application Number : 208476

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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05

Brand Name : SOLIFENACIN SUCCINAT...

BioFlorida Conference
Not Confirmed
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Brand Name : SOLIFENACIN SUCCINAT...

BioFlorida Conference
Not Confirmed
arrow

AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : SOLIFENACIN SUCCINATE

Dosage Strength : 5MG

Approval Date : 2019-05-20

Application Number : 210281

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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06

Brand Name : SOLIFENACIN SUCCINAT...

BioFlorida Conference
Not Confirmed
arrow

Brand Name : SOLIFENACIN SUCCINAT...

BioFlorida Conference
Not Confirmed
arrow

AustarPharma

Dosage Form : TABLET; ORAL

Proprietary Name : SOLIFENACIN SUCCINATE

Dosage Strength : 10MG

Approval Date : 2019-05-20

Application Number : 210281

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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