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Approved Drug Products containing 205761 listed in the FDA Orange Book. Original Data : FDA Website

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01 1AUROBINDO PHARMA

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01

Brand Name : RABEPRAZOLE SODIUM

FNCE 2024
Not Confirmed
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Brand Name : RABEPRAZOLE SODIUM

FNCE 2024
Not Confirmed
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Aurobindo Pharma Limited

Dosage Form : TABLET, DELAYED RELEASE; ORAL

Proprietary Name : RABEPRAZOLE SODIUM

Dosage Strength : 20MG

Approval Date : 2017-02-17

Application Number : 205761

RX/OTC/DISCN : RX

RLD : No

TE Code : AB

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