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01 3PRINSTON INC
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01 3TABLET, DELAYED RELEASE;ORAL
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01 3RX
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01 3DIVALPROEX SODIUM
01 3No
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RLD : No
TE Code : AB
Dosage Form : TABLET, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 500MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
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, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 125MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
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, DELAYED RELEASE; ORAL
Proprietary Name : DIVALPROEX SODIUM
Dosage Strength : EQ 250MG VALPROIC ACID
Approval Date : 2009-11-30
Application Number : 90210
RX/OTC/DISCN : RX
RLD : No
TE Code : AB
