<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
79706-001-01
</NDCCode>
<PackageDescription>
10869 TABLET in 1 PAIL (79706-001-01)
</PackageDescription>
<NDC11Code>
79706-0001-01
</NDC11Code>
<ProductNDC>
79706-001
</ProductNDC>
<ProductTypeName>
DRUG FOR FURTHER PROCESSING
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Phenylephrinehydrochloride,guaifenesin
</NonProprietaryName>
<DosageFormName>
TABLET
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20250318
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
Ameripharma Labs Limited Liability Company
</LabelerName>
<SubstanceName>
PHENYLEPHRINE HYDROCHLORIDE; GUAIFENESIN
</SubstanceName>
<StrengthNumber>
390; 10
</StrengthNumber>
<StrengthUnit>
mg/1; mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Unfinished
</Status>
<LastUpdate>
2026-08-07
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20271231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
18-MAR-25
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>