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Approved Drug Products containing 90776 listed in the FDA Orange Book. Original Data : FDA Website

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01 3ACTAVIS ELIZABETH

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PharmaCompass

01

Brand Name : DULOXETINE HYDROCHLO...

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Not Confirmed
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Brand Name : DULOXETINE HYDROCHLO...

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Not Confirmed
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Actavis Inc

Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

Proprietary Name : DULOXETINE HYDROCHLORIDE

Dosage Strength : EQ 20MG BASE

Approval Date : 2013-12-17

Application Number : 90776

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : DULOXETINE HYDROCHLO...

Luxepack
Not Confirmed
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Brand Name : DULOXETINE HYDROCHLO...

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

Proprietary Name : DULOXETINE HYDROCHLORIDE

Dosage Strength : EQ 30MG BASE

Approval Date : 2013-12-17

Application Number : 90776

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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03

Brand Name : DULOXETINE HYDROCHLO...

Luxepack
Not Confirmed
arrow

Brand Name : DULOXETINE HYDROCHLO...

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : CAPSULE, DELAYED REL PELLETS; ...

Proprietary Name : DULOXETINE HYDROCHLORIDE

Dosage Strength : EQ 60MG BASE

Approval Date : 2013-12-17

Application Number : 90776

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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