{
"NDC": {
"NDCCode": "69844-024-02",
"PackageDescription": "60 TABLET in 1 BOTTLE (69844-024-02) ",
"NDC11Code": "69844-0024-02",
"ProductNDC": "69844-024",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ranolazine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Extended-release",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20210128",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA212889",
"LabelerName": "Graviti Pharmaceuticals Private Limited",
"SubstanceName": "RANOLAZINE",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-05-20",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20210128",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}