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01 2LUPIN LTD
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01 2TABLET, EXTENDED RELEASE;ORAL
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01 2RX
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01 2DIVALPROEX SODIUM
01 2No
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RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 250MG VALPROIC ACID
Approval Date : 2019-10-18
Application Number : 209286
RX/OTC/DISCN : RX
RLD : No
TE Code : AB

Boost your online visibility by uploading your products, APIs, FDFs, intermediates, excipients, and services for free on PharmaCompass.
Rank higher among suppliers and expand your reach across the internet efficiently and cost-effectively.
RLD : No
TE Code : AB
Dosage Form : TABLET, EXTENDED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 500MG VALPROIC ACID
Approval Date : 2019-10-18
Application Number : 209286
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
