<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
54348-015-01
</NDCCode>
<PackageDescription>
1 BLISTER PACK in 1 BOX (54348-015-01) > 1 TABLET in 1 BLISTER PACK
</PackageDescription>
<NDC11Code>
54348-0015-01
</NDC11Code>
<ProductNDC>
54348-015
</ProductNDC>
<ProductTypeName>
HUMAN PRESCRIPTION DRUG
</ProductTypeName>
<ProprietaryName>
Acetaminophen With Codeine
</ProprietaryName>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Acetaminophen, Codeine Phosphate
</NonProprietaryName>
<DosageFormName>
TABLET
</DosageFormName>
<RouteName>
ORAL
</RouteName>
<StartMarketingDate>
20131231
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
ANDA
</MarketingCategoryName>
<ApplicationNumber>
ANDA089805
</ApplicationNumber>
<LabelerName>
PharmPak, Inc.
</LabelerName>
<SubstanceName>
CODEINE PHOSPHATE; ACETAMINOPHEN
</SubstanceName>
<StrengthNumber>
30; 300
</StrengthNumber>
<StrengthUnit>
mg/1; mg/1
</StrengthUnit>
<Pharm_Classes>
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
</Pharm_Classes>
<DEASchedule>
CIII
</DEASchedule>
<Status>
Deprecated
</Status>
<LastUpdate>
2019-09-21
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag>
E
</ProductNdcExcludeFlag>
<ListingRecordCertifiedThrough>
20171231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage/>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>