{
"NDC": {
"NDCCode": "44224-0118-1",
"PackageDescription": "1 KIT in 1 KIT (44224-0118-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .5 g in 1 TUBE (52124-0003-1) * 2 TABLET, FILM COATED in 1 PACKET (47682-116-99) * 1 CAPSULE in 1 PACKET (47682-182-46) * 2 TABLET, FILM COATED in 1 PACKET (47682-808-99) * 2 TABLET, FILM COATED in 1 PACKET (47682-145-99) * 22 g in 1 PACKET (52380-0001-3)",
"NDC11Code": "44224-0118-01",
"ProductNDC": "44224-0118",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Mountain Series Weekender Medical",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benzalkonium Chloride, Povidone-iodine, Acetaminophen, Aspirin, Diphenhydramine Hydrochloride, Ibuprofen, Bacitracin Zinc, Neomycin Sulfate, Polymyxin B Sulfate",
"DosageFormName": "KIT",
"RouteName": null,
"StartMarketingDate": "20110801",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part333A",
"LabelerName": "Tender Corporation dba Adventure Medical Kits",
"SubstanceName": null,
"StrengthNumber": null,
"StrengthUnit": null,
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}