<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
51552-0907-4
</NDCCode>
<PackageDescription>
25 g in 1 CONTAINER (51552-0907-4)
</PackageDescription>
<NDC11Code>
51552-0907-04
</NDC11Code>
<ProductNDC>
51552-0907
</ProductNDC>
<ProductTypeName>
BULK INGREDIENT
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Butalbital
</NonProprietaryName>
<DosageFormName>
POWDER
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20090104
</StartMarketingDate>
<EndMarketingDate>
20260818
</EndMarketingDate>
<MarketingCategoryName>
BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
Fagron Inc
</LabelerName>
<SubstanceName>
BUTALBITAL
</SubstanceName>
<StrengthNumber>
1
</StrengthNumber>
<StrengthUnit>
g/g
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule>
CIII
</DEASchedule>
<Status>
Unfinished
</Status>
<LastUpdate>
2024-12-13
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage>
04-JAN-09
</StartMarketingDatePackage>
<EndMarketingDatePackage>
18-AUG-26
</EndMarketingDatePackage>
<SamplePackage/>
</NDC>