<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
67296-1427-2
</NDCCode>
<PackageDescription>
20 TABLET in 1 BOTTLE (67296-1427-2)
</PackageDescription>
<NDC11Code>
67296-1427-02
</NDC11Code>
<ProductNDC>
67296-1427
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Phenobarbital
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Phenobarbital
</NonProprietaryName>
<DosageFormName>
TABLET
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20190521
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
UNAPPROVED DRUG OTHER
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
RedPharm Drug, Inc.
</LabelerName>
<SubstanceName>
PHENOBARBITAL
</SubstanceName>
<StrengthNumber>
32.4
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule>
CIV
</DEASchedule>
<Status>
Deprecated
</Status>
<LastUpdate>
2026-01-01
</LastUpdate>
<PackageNdcExcludeFlag>
N
</PackageNdcExcludeFlag>
<ProductNdcExcludeFlag>
N
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20251231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
20210301
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage>
N
</SamplePackage>
</NDC>