{
"NDC": {
"NDCCode": "54569-6227-0",
"PackageDescription": "30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (54569-6227-0)",
"NDC11Code": "54569-6227-00",
"ProductNDC": "54569-6227",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Venlafaxine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Venlafaxine Hydrochloride",
"DosageFormName": "CAPSULE, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20100701",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076565",
"LabelerName": "A-S Medication Solutions",
"SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
"StrengthNumber": "150",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-01-10",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}