{
"NDC": {
"NDCCode": "65219-622-10",
"PackageDescription": "10 VIAL in 1 CARTON (65219-622-10) / 10 mL in 1 VIAL (65219-622-02) ",
"NDC11Code": "65219-0622-10",
"ProductNDC": "65219-622",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Acyclovir",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Acyclovir",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20241216",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA215404",
"LabelerName": "Fresenius Kabi USA, LLC",
"SubstanceName": "ACYCLOVIR SODIUM",
"StrengthNumber": "50",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "DNA Polymerase Inhibitors [MoA], Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC], Nucleoside Analog [EXT]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2024-12-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20241216",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}