{
"NDC": {
"NDCCode": "60687-237-25",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-237-25) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-237-95) ",
"NDC11Code": "60687-0237-25",
"ProductNDC": "60687-237",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Propranolol Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Propranolol Hydrochloride",
"DosageFormName": "CAPSULE, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20170224",
"EndMarketingDate": "20181031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078703",
"LabelerName": "American Health Packaging",
"SubstanceName": "PROPRANOLOL HYDROCHLORIDE",
"StrengthNumber": "120",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-11-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20170224",
"EndMarketingDatePackage": "20181031",
"SamplePackage": "N"
}
}