{
"NDC": {
"NDCCode": "75826-112-00",
"PackageDescription": "1000 TABLET in 1 BOTTLE, PLASTIC (75826-112-00)",
"NDC11Code": "75826-0112-00",
"ProductNDC": "75826-112",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "B-donna",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20151230",
"EndMarketingDate": null,
"MarketingCategoryName": "UNAPPROVED DRUG OTHER",
"ApplicationNumber": null,
"LabelerName": "Winder Laboratories, LLC",
"SubstanceName": "PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE",
"StrengthNumber": "16.2; .1037; .0194; .0065",
"StrengthUnit": "mg/1; mg/1; mg/1; mg/1",
"Pharm_Classes": "Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-03-11",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}