Current NDC auxiliary source row compounder:723

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: 83155-100
Product Ndc: 83155-100
Product Ndc Digits: 83155100
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Sodium Chloride
Proprietary Name Suffix: [empty]
Nonproprietary Name: Sodium Chloride
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Assure Infusions Inc
Establishment Name: Assure Infusions Inc
Establishment Fei: [empty]
Substance Name: SODIUM CHLORIDE
Active Ingredients Info: 900 mg/100 mL
History Active Ingredients Raw: SODIUM CHLORIDE
History Active Ingredients Info Raw: 900 mg/100 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 83155-100-50
Package Ndc: 83155-100-50
Package Ndc Digits: 8315510050
Package Ndc11: 83155010050
Package Description: 500 mL in 1 BAG (83155-100-50)
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:723
Source Row Number: 723
Source Row Hash: 63f1c414a58f0fabae2be25a04985263f6abd1b4609444df259aaed684c59554
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "83155-100",
    "DEASCHEDULE": "",
    "LABELERNAME": "Assure Infusions Inc",
    "SUBSTANCENAME": "SODIUM CHLORIDE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "83155-100-50",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Sodium Chloride",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Sodium Chloride",
    "PACKAGEDESCRIPTION": "500 mL in 1 BAG (83155-100-50) ",
    "ACTIVEINGREDIENTSINFO": "900 mg/100 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:723
Source Row Number: 723
Status Scope: package
Lookup Ndc: 83155-100-50
Lookup Ndc Digits: 8315510050
Product Ndc: 83155-100
Product Ndc Digits: 83155100
Package Ndc: 83155-100-50
Package Ndc Digits: 8315510050
Package Ndc11: 83155010050
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: 63f1c414a58f0fabae2be25a04985263f6abd1b4609444df259aaed684c59554
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51