{
"NDC": {
"NDCCode": "60687-306-01",
"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-306-01) > 1 TABLET in 1 BLISTER PACK (60687-306-11) ",
"NDC11Code": "60687-0306-01",
"ProductNDC": "60687-306",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Propranolol Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Propranolol Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20170715",
"EndMarketingDate": "20220930",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA070176",
"LabelerName": "American Health Packaging",
"SubstanceName": "PROPRANOLOL HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-10-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20170715",
"EndMarketingDatePackage": "20220930",
"SamplePackage": "N"
}
}