{
"NDC": {
"NDCCode": "80425-0452-1",
"PackageDescription": "1 TUBE, WITH APPLICATOR in 1 BOX (80425-0452-1) / 9900 mg in 1 TUBE, WITH APPLICATOR",
"NDC11Code": "80425-0452-01",
"ProductNDC": "80425-0452",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lidopro Pain Relief",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Capsaicin And Lidocaine",
"DosageFormName": "OINTMENT",
"RouteName": "TRANSDERMAL",
"StartMarketingDate": "20241126",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH DRUG",
"ApplicationNumber": "M017",
"LabelerName": "Advanced Rx of Tennessee, LLC",
"SubstanceName": "CAPSAICIN; LIDOCAINE HYDROCHLORIDE; MENTHOL, (+)-; METHYL SALICYLATE",
"StrengthNumber": ".0325; 4; 10; 27.5",
"StrengthUnit": "mg/100mg; mg/100mg; mg/100mg; mg/100mg",
"Pharm_Classes": "Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-01-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20241126",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}