Current NDC auxiliary source row compounder:215

This page is keyed by dataset, FDA.report source record ID, and physical source row number. Empty values are shown rather than omitted.

Complete normalized row#

Record Source: ndc_compounder_zip
Product Ndc Raw: 68985-486
Product Ndc: 68985-486
Product Ndc Digits: 68985486
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: LIDOCAINE 40MG
Proprietary Name Suffix: [empty]
Nonproprietary Name: LIDOCAINE 40MG
Dosage Form Name: SOLUTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: LEESAR INC
Establishment Name: LEESAR INC
Establishment Fei: [empty]
Substance Name: LIDOCAINE HYDROCHLORIDE ANHYDROUS; LIDOCAINE HYDROCHLORIDE
Active Ingredients Info: 20 mg/1 mL; 20 mg/1 mL
History Active Ingredients Raw: LIDOCAINE HYDROCHLORIDE ANHYDROUS; LIDOCAINE HYDROCHLORIDE
History Active Ingredients Info Raw: 20 mg/1 mL; 20 mg/1 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 68985-486-93
Package Ndc: 68985-486-93
Package Ndc Digits: 6898548693
Package Ndc11: 68985048693
Package Description: 3 mL in 1 SYRINGE (68985-486-93)
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Normalization Status: valid
Source Url: https://www.accessdata.fda.gov/cder/compounders_ndc_directory.zip
Source Archive: compounders_ndc_directory.zip
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Last Modified: Fri, 18 Sep 2026 15:17:23 GMT
Source Archive Sha256: 222f6800f79cb1a0fa79431b7226bd6b34899999dbf086af51004a96774ada98
Source Member Sha256: f8d9743e5616579a34d614887e86a53913efa0a63d3138d59d2f87cbb4d0cc17
Source Record Id: compounder:215
Source Row Number: 215
Source Row Hash: 9939abb882bfd16da63916c7c839e75d38644caefffd9bdd943607af7c232e43
Import Run Id: 20261022T045816Z
Loaded At: 2026-10-22 05:03:38

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "68985-486",
    "DEASCHEDULE": "",
    "LABELERNAME": "LEESAR INC",
    "SUBSTANCENAME": "LIDOCAINE HYDROCHLORIDE ANHYDROUS; LIDOCAINE HYDROCHLORIDE",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "68985-486-93",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "LIDOCAINE 40MG",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "LIDOCAINE 40MG",
    "PACKAGEDESCRIPTION": "3 mL in 1 SYRINGE (68985-486-93) ",
    "ACTIVEINGREDIENTSINFO": "20 mg/1 mL; 20 mg/1 mL",
    "MARKETINGCATEGORYNAME": "OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)",
    "PROPRIETARYNAMESUFFIX": ""
}

Normalization notes#

[]

Current status projection#

Dataset: compounder
Record Source: ndc_compounder_zip
Source Record Id: compounder:215
Source Row Number: 215
Status Scope: package
Lookup Ndc: 68985-486-93
Lookup Ndc Digits: 6898548693
Product Ndc: 68985-486
Product Ndc Digits: 68985486
Package Ndc: 68985-486-93
Package Ndc Digits: 6898548693
Package Ndc11: 68985048693
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 9939abb882bfd16da63916c7c839e75d38644caefffd9bdd943607af7c232e43
Import Run Id: 20261022T045816Z
Loaded At: 2026-10-22 05:03:38