Current NDC auxiliary source row compounder:2155

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: 69374-984
Product Ndc: 69374-984
Product Ndc Digits: 69374984
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: del Nido Cardioplegia
Proprietary Name Suffix: [empty]
Nonproprietary Name: del Nido Cardioplegia
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRACARDIAC
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Nephron Sterile Compounding Center, LLC
Establishment Name: Nephron Sterile Compounding Center, LLC
Establishment Fei: [empty]
Substance Name: SODIUM BICARBONATE; LIDOCAINE HYDROCHLORIDE; POTASSIUM CHLORIDE
Active Ingredients Info: 1.04 g/1 mL; 123 mg/1 mL; 2.19 g/1 mL
History Active Ingredients Raw: SODIUM BICARBONATE; LIDOCAINE HYDROCHLORIDE; POTASSIUM CHLORIDE
History Active Ingredients Info Raw: 1.04 g/1 mL; 123 mg/1 mL; 2.19 g/1 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 69374-984-10
Package Ndc: 69374-984-10
Package Ndc Digits: 6937498410
Package Ndc11: 69374098410
Package Description: 4 BAG in 1 CASE (69374-984-10) > 1000 mL in 1 BAG
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
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:2155
Source Row Number: 2155
Source Row Hash: 86f91c2c343aaa91c9b7541cd4d6726e06ad1a29adbd07701b69042864af15eb
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRACARDIAC",
    "PRODUCTNDC": "69374-984",
    "DEASCHEDULE": "",
    "LABELERNAME": "Nephron Sterile Compounding Center, LLC",
    "SUBSTANCENAME": "SODIUM BICARBONATE; LIDOCAINE HYDROCHLORIDE; POTASSIUM CHLORIDE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "69374-984-10",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "del Nido Cardioplegia",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "del Nido Cardioplegia",
    "PACKAGEDESCRIPTION": "4 BAG in 1 CASE (69374-984-10)  > 1000 mL in 1 BAG",
    "ACTIVEINGREDIENTSINFO": "1.04 g/1 mL; 123 mg/1 mL; 2.19 g/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:2155
Source Row Number: 2155
Status Scope: package
Lookup Ndc: 69374-984-10
Lookup Ndc Digits: 6937498410
Product Ndc: 69374-984
Product Ndc Digits: 69374984
Package Ndc: 69374-984-10
Package Ndc Digits: 6937498410
Package Ndc11: 69374098410
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 86f91c2c343aaa91c9b7541cd4d6726e06ad1a29adbd07701b69042864af15eb
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01