{
"NDC": {
"NDCCode": "70518-0833-2",
"PackageDescription": "100 POUCH in 1 BOX (70518-0833-2) > 1 TABLET in 1 POUCH (70518-0833-1) ",
"NDC11Code": "70518-0833-02",
"ProductNDC": "70518-0833",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Propranolol Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Propranolol Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20171109",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA070178",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "PROPRANOLOL HYDROCHLORIDE",
"StrengthNumber": "80",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-02-23",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20190521",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}