<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
0074-7345-99
</NDCCode>
<PackageDescription>
20000 TABLET, DELAYED RELEASE in 1 DRUM (0074-7345-99)
</PackageDescription>
<NDC11Code>
00074-7345-99
</NDC11Code>
<ProductNDC>
0074-7345
</ProductNDC>
<ProductTypeName>
DRUG FOR FURTHER PROCESSING
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Divalproex Sodium
</NonProprietaryName>
<DosageFormName>
TABLET, DELAYED RELEASE
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20260922
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
AbbVie Inc.
</LabelerName>
<SubstanceName>
DIVALPROEX SODIUM
</SubstanceName>
<StrengthNumber>
125
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Unfinished
</Status>
<LastUpdate>
2026-10-06
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20271231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
22-SEP-26
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>