Current NDC auxiliary source row compounder:587

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: 81483-0044
Product Ndc: 81483-0044
Product Ndc Digits: 814830044
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Albuterol Sulfate
Proprietary Name Suffix: [empty]
Nonproprietary Name: Albuterol Sulfate
Dosage Form Name: INHALANT
Route Name: RESPIRATORY (INHALATION)
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: TAILSTORM HEALTH INC
Establishment Name: TAILSTORM HEALTH INC
Establishment Fei: [empty]
Substance Name: ALBUTEROL SULFATE
Active Ingredients Info: 5 mg/1 mL
History Active Ingredients Raw: ALBUTEROL SULFATE
History Active Ingredients Info Raw: 5 mg/1 mL
History Dosage Raw: INHALANT
Dea Schedule: [empty]
Package Ndc Raw: 81483-0044-0
Package Ndc: 81483-0044-0
Package Ndc Digits: 8148300440
Package Ndc11: 81483004400
Package Description: 25 VIAL in 1 TRAY (81483-0044-0) > 10 mL in 1 VIAL
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:587
Source Row Number: 587
Source Row Hash: c1ce98b182bb782ef2c751edcce26b21aafb0ded1883e8b5886fb2d0a06b620b
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "RESPIRATORY (INHALATION)",
    "PRODUCTNDC": "81483-0044",
    "DEASCHEDULE": "",
    "LABELERNAME": "TAILSTORM HEALTH INC",
    "SUBSTANCENAME": "ALBUTEROL SULFATE",
    "DOSAGEFORMNAME": "INHALANT",
    "NDCPACKAGECODE": "81483-0044-0",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Albuterol Sulfate",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "Albuterol Sulfate",
    "PACKAGEDESCRIPTION": "25 VIAL in 1 TRAY (81483-0044-0)  > 10 mL in 1 VIAL",
    "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:587
Source Row Number: 587
Status Scope: package
Lookup Ndc: 81483-0044-0
Lookup Ndc Digits: 8148300440
Product Ndc: 81483-0044
Product Ndc Digits: 814830044
Package Ndc: 81483-0044-0
Package Ndc Digits: 8148300440
Package Ndc11: 81483004400
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: c1ce98b182bb782ef2c751edcce26b21aafb0ded1883e8b5886fb2d0a06b620b
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20