<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
10888-8175-1
</NDCCode>
<PackageDescription>
10000 TABLET, EXTENDED RELEASE in 1 CASE (10888-8175-1)
</PackageDescription>
<NDC11Code>
10888-8175-01
</NDC11Code>
<ProductNDC>
10888-8175
</ProductNDC>
<ProductTypeName>
DRUG FOR FURTHER PROCESSING
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Acetaminophen
</NonProprietaryName>
<DosageFormName>
TABLET, EXTENDED RELEASE
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20121114
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
Patheon Softgels Inc.
</LabelerName>
<SubstanceName>
ACETAMINOPHEN
</SubstanceName>
<StrengthNumber>
650
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Unfinished
</Status>
<LastUpdate>
2021-09-23
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20221231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
14-NOV-12
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>