Current NDC auxiliary source row compounder:359

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: 72790-004
Product Ndc: 72790-004
Product Ndc Digits: 72790004
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Non-proprietary
Proprietary Name Suffix: [empty]
Nonproprietary Name: Ethanol
Dosage Form Name: INJECTION
Route Name: EXTRACORPOREAL
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Molecular PharmaGroup
Establishment Name: Molecular PharmaGroup
Establishment Fei: [empty]
Substance Name: DEHYDRATED ALCOHOL
Active Ingredients Info: 2.1 mL/3 mL
History Active Ingredients Raw: DEHYDRATED ALCOHOL
History Active Ingredients Info Raw: 2.1 mL/3 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 72790-004-05
Package Ndc: 72790-004-05
Package Ndc Digits: 7279000405
Package Ndc11: 72790000405
Package Description: 10 SYRINGE in 1 BOX (72790-004-05) > 3 mL in 1 SYRINGE (72790-004-01)
Reporting Period Raw: 2025-2
Reporting Period: 2025-2
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:359
Source Row Number: 359
Source Row Hash: be4ba8815a2b8bb24279060a55524f1c0d44b57e23c9e4439ba2b4fedad5304b
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "EXTRACORPOREAL",
    "PRODUCTNDC": "72790-004",
    "DEASCHEDULE": "",
    "LABELERNAME": "Molecular PharmaGroup",
    "SUBSTANCENAME": "DEHYDRATED ALCOHOL",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "72790-004-05",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Non-proprietary",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "Ethanol",
    "PACKAGEDESCRIPTION": "10 SYRINGE in 1 BOX (72790-004-05)  > 3 mL in 1 SYRINGE (72790-004-01) ",
    "ACTIVEINGREDIENTSINFO": "2.1 mL/3 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:359
Source Row Number: 359
Status Scope: package
Lookup Ndc: 72790-004-05
Lookup Ndc Digits: 7279000405
Product Ndc: 72790-004
Product Ndc Digits: 72790004
Package Ndc: 72790-004-05
Package Ndc Digits: 7279000405
Package Ndc11: 72790000405
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2025-2
Reporting Period: 2025-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: be4ba8815a2b8bb24279060a55524f1c0d44b57e23c9e4439ba2b4fedad5304b
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20