{
"NDC": {
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"PackageDescription": "1000 TABLET in 1 BOTTLE (60258-850-10)",
"NDC11Code": "60258-0850-10",
"ProductNDC": "60258-850",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Cyproheptadine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Cyproheptadine Hydrochloride",
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"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040644",
"LabelerName": "Cypress Pharmaceutical, Inc.",
"SubstanceName": "CYPROHEPTADINE HYDROCHLORIDE",
"StrengthNumber": "4",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2015-01-16",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}