Current NDC auxiliary source row compounder:3531

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: 69374-330
Product Ndc: 69374-330
Product Ndc Digits: 69374330
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Albuterol Sulfate 0.5%
Proprietary Name Suffix: [empty]
Nonproprietary Name: Albuterol Sulfate 0.5%
Dosage Form Name: SOLUTION
Route Name: RESPIRATORY (INHALATION)
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: ALBUTEROL
Active Ingredients Info: 5 mg/1 mL
History Active Ingredients Raw: ALBUTEROL
History Active Ingredients Info Raw: 5 mg/1 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 69374-330-05
Package Ndc: 69374-330-05
Package Ndc Digits: 6937433005
Package Ndc11: 69374033005
Package Description: 30 CARTON in 1 CASE (69374-330-05) > 30 VIAL, PLASTIC in 1 CARTON > 5 mL in 1 VIAL, PLASTIC
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
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:3531
Source Row Number: 3531
Source Row Hash: e629214f8e6e2a65ff5db9d728ed84c162fd84cee03e595c6d21e166797df34f
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27

Exact raw FDA source fields#

{
    "ROUTENAME": "RESPIRATORY (INHALATION)",
    "PRODUCTNDC": "69374-330",
    "DEASCHEDULE": "",
    "LABELERNAME": "Nephron Sterile Compounding Center, LLC",
    "SUBSTANCENAME": "ALBUTEROL",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "69374-330-05",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Albuterol Sulfate 0.5%",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Albuterol Sulfate 0.5%",
    "PACKAGEDESCRIPTION": "30 CARTON in 1 CASE (69374-330-05)  > 30 VIAL, PLASTIC in 1 CARTON > 5 mL in 1 VIAL, PLASTIC",
    "ACTIVEINGREDIENTSINFO": "5 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:3531
Source Row Number: 3531
Status Scope: package
Lookup Ndc: 69374-330-05
Lookup Ndc Digits: 6937433005
Product Ndc: 69374-330
Product Ndc Digits: 69374330
Package Ndc: 69374-330-05
Package Ndc Digits: 6937433005
Package Ndc11: 69374033005
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: e629214f8e6e2a65ff5db9d728ed84c162fd84cee03e595c6d21e166797df34f
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27