{
"NDC": {
"NDCCode": "51079-576-20",
"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-576-20) > 1 TABLET in 1 BLISTER PACK (51079-576-01)",
"NDC11Code": "51079-0576-20",
"ProductNDC": "51079-576",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Pramipexole Dihydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Pramipexole Dihydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20101117",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077854",
"LabelerName": "UDL Laboratories, Inc.",
"SubstanceName": "PRAMIPEXOLE DIHYDROCHLORIDE",
"StrengthNumber": ".125",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2014-03-05",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}