{
"NDC": {
"NDCCode": "83270-003-01",
"PackageDescription": "500 mg in 1 VIAL (83270-003-01) ",
"NDC11Code": "83270-0003-01",
"ProductNDC": "83270-003",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Methohexital Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Methohexital Sodium",
"DosageFormName": "INJECTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20241212",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA215488",
"LabelerName": "ONESOURCE SPECIALTY PHARMA LIMITED",
"SubstanceName": "METHOHEXITAL SODIUM",
"StrengthNumber": "500",
"StrengthUnit": "mg/500mg",
"Pharm_Classes": "Barbiturate [EPC], Barbiturates [CS]",
"DEASchedule": "CIV",
"Status": "Active",
"LastUpdate": "2025-05-23",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20241212",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}