{
"NDC": {
"NDCCode": "73293-0002-2",
"PackageDescription": "50 AMPULE in 1 PACKAGE (73293-0002-2) / 2 mL in 1 AMPULE (73293-0002-1) ",
"NDC11Code": "73293-0002-02",
"ProductNDC": "73293-0002",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Bupivacaine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Bupivacaine Hydrochloride",
"DosageFormName": "INJECTION",
"RouteName": "SUBARACHNOID",
"StartMarketingDate": "20191230",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA212822",
"LabelerName": "Huons Co., Ltd.",
"SubstanceName": "BUPIVACAINE HYDROCHLORIDE",
"StrengthNumber": "7.5",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Local Anesthesia [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-02-19",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20191230",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}