{
"NDC": {
"NDCCode": "10019-510-01",
"PackageDescription": "10 VIAL, SINGLE-DOSE in 1 PACKAGE (10019-510-01) > 5 mL in 1 VIAL, SINGLE-DOSE (10019-510-79)",
"NDC11Code": "10019-0510-01",
"ProductNDC": "10019-510",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Diltiazem Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Diltiazem Hydrochloride",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20100713",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078538",
"LabelerName": "Baxter Healthcare Corporation",
"SubstanceName": "DILTIAZEM HYDROCHLORIDE",
"StrengthNumber": "5",
"StrengthUnit": "mg/mL",
"Pharm_Classes": "Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2015-08-14",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}