Current NDC auxiliary source row compounder:256

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: 72627-2404
Product Ndc: 72627-2404
Product Ndc Digits: 726272404
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Ascorbic Acid
Proprietary Name Suffix: [empty]
Nonproprietary Name: Ascorbic Acid
Dosage Form Name: INJECTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Empower Pharma
Establishment Name: Empower Pharma
Establishment Fei: [empty]
Substance Name: ASCORBIC ACID
Active Ingredients Info: 500 mg/1 mL
History Active Ingredients Raw: ASCORBIC ACID
History Active Ingredients Info Raw: 500 mg/1 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 72627-2404-1
Package Ndc: 72627-2404-1
Package Ndc Digits: 7262724041
Package Ndc11: 72627240401
Package Description: 30 mL in 1 VIAL, SINGLE-DOSE (72627-2404-1)
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:256
Source Row Number: 256
Source Row Hash: a194872d8c7764f75ef2c5bd5b0eb3d3a16dd7fca9958e3d03cfa98f20383d25
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "72627-2404",
    "DEASCHEDULE": "",
    "LABELERNAME": "Empower Pharma",
    "SUBSTANCENAME": "ASCORBIC ACID",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "72627-2404-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Ascorbic Acid",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Ascorbic Acid",
    "PACKAGEDESCRIPTION": "30 mL in 1 VIAL, SINGLE-DOSE (72627-2404-1) ",
    "ACTIVEINGREDIENTSINFO": "500 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:256
Source Row Number: 256
Status Scope: package
Lookup Ndc: 72627-2404-1
Lookup Ndc Digits: 7262724041
Product Ndc: 72627-2404
Product Ndc Digits: 726272404
Package Ndc: 72627-2404-1
Package Ndc Digits: 7262724041
Package Ndc11: 72627240401
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: a194872d8c7764f75ef2c5bd5b0eb3d3a16dd7fca9958e3d03cfa98f20383d25
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57