{
"NDC": {
"NDCCode": "50090-3490-0",
"PackageDescription": "33 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-3490-0) ",
"NDC11Code": "50090-3490-00",
"ProductNDC": "50090-3490",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lithium Carbonate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lithium Carbonate",
"DosageFormName": "TABLET, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20171201",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA205663",
"LabelerName": "A-S Medication Solutions",
"SubstanceName": "LITHIUM CARBONATE",
"StrengthNumber": "450",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Mood Stabilizer [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180618",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}