{
"NDC": {
"NDCCode": "0085-0492-01",
"PackageDescription": "100 TABLET in 1 BOTTLE (0085-0492-01) ",
"NDC11Code": "00085-0492-01",
"ProductNDC": "0085-0492",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Guanidine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Guanidine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19391002",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA001546",
"LabelerName": "Merck Sharp & Dohme Corp.",
"SubstanceName": "GUANIDINE HYDROCHLORIDE",
"StrengthNumber": "125",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Acetylcholine Releasing Agent [EPC],Increased Acetylcholine Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-09-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20211231",
"StartMarketingDatePackage": "19391002",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}