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Approved Drug Products containing 90797 listed in the FDA Orange Book. Original Data : FDA Website

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01 2ACTAVIS TOTOWA

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PharmaCompass

01

Brand Name : PANTOPRAZOLE SODIUM

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Not Confirmed
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Brand Name : PANTOPRAZOLE SODIUM

Luxepack
Not Confirmed
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Actavis Inc

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Proprietary Name : PANTOPRAZOLE SODIUM

Dosage Strength : EQ 20MG BASE

Approval Date : 2011-02-07

Application Number : 90797

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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02

Brand Name : PANTOPRAZOLE SODIUM

Luxepack
Not Confirmed
arrow

Brand Name : PANTOPRAZOLE SODIUM

Luxepack
Not Confirmed
arrow

Actavis Inc

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Proprietary Name : PANTOPRAZOLE SODIUM

Dosage Strength : EQ 40MG BASE

Approval Date : 2011-02-07

Application Number : 90797

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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