<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
70120-123-30
</NDCCode>
<PackageDescription>
20000 TABLET, FILM COATED in 1 BAG (70120-123-30)
</PackageDescription>
<NDC11Code>
70120-0123-30
</NDC11Code>
<ProductNDC>
70120-123
</ProductNDC>
<ProductTypeName>
DRUG FOR FURTHER PROCESSING
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Gabapentin
</NonProprietaryName>
<DosageFormName>
TABLET, FILM COATED
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20200214
</StartMarketingDate>
<EndMarketingDate>
20230131
</EndMarketingDate>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
APL HEALTHCARE LIMITED
</LabelerName>
<SubstanceName>
GABAPENTIN
</SubstanceName>
<StrengthNumber>
600
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Deprecated
</Status>
<LastUpdate>
2014-02-04
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough/>
<StartMarketingDatePackage>
07-MAY-20
</StartMarketingDatePackage>
<EndMarketingDatePackage>
31-JAN-23
</EndMarketingDatePackage>
<SamplePackage/>
</NDC>