{
"NDC": {
"NDCCode": "71890-310-01",
"PackageDescription": "1 TUBE in 1 BOX (71890-310-01) > 44.3603 mL in 1 TUBE",
"NDC11Code": "71890-0310-01",
"ProductNDC": "71890-310",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Lidoforte Hemorrhoidal",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lidocaine Mineral Phenylephrine Hydrochloride Petrolatum",
"DosageFormName": "CREAM",
"RouteName": "TOPICAL",
"StartMarketingDate": "20171118",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part346",
"LabelerName": "Satius Pharmaceuticals, LLC",
"SubstanceName": "LIDOCAINE; MINERAL OIL; PETROLATUM; PHENYLEPHRINE HYDROCHLORIDE",
"StrengthNumber": "50; 170; 390; 25",
"StrengthUnit": "mg/mL; mg/mL; mg/mL; mg/mL",
"Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE], alpha-1 Adrenergic Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-10-10",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}