Current NDC auxiliary source row compounder:950

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: 72682-2243
Product Ndc: 72682-2243
Product Ndc Digits: 726822243
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Ascorbic Acid (PF/Non-Corn) 500 mg/ml 10mL Refrig
Proprietary Name Suffix: [empty]
Nonproprietary Name: Ascorbic Acid (PF/Non-Corn) 500 mg/ml 10mL Refrig
Dosage Form Name: INJECTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: AnazaoHealth Corporation
Establishment Name: AnazaoHealth Corporation
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: 72682-2243-1
Package Ndc: 72682-2243-1
Package Ndc Digits: 7268222431
Package Ndc11: 72682224301
Package Description: 10 mL in 1 VIAL (72682-2243-1)
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:950
Source Row Number: 950
Source Row Hash: dde472a7aa83a46122f0c25379b11e923d82501c9eca4e9035637e65a4d7cf36
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "72682-2243",
    "DEASCHEDULE": "",
    "LABELERNAME": "AnazaoHealth Corporation",
    "SUBSTANCENAME": "ASCORBIC ACID",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "72682-2243-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Ascorbic Acid (PF/Non-Corn) 500 mg/ml 10mL Refrig",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Ascorbic Acid (PF/Non-Corn) 500 mg/ml 10mL Refrig",
    "PACKAGEDESCRIPTION": "10 mL in 1 VIAL (72682-2243-1) ",
    "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:950
Source Row Number: 950
Status Scope: package
Lookup Ndc: 72682-2243-1
Lookup Ndc Digits: 7268222431
Product Ndc: 72682-2243
Product Ndc Digits: 726822243
Package Ndc: 72682-2243-1
Package Ndc Digits: 7268222431
Package Ndc11: 72682224301
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: dde472a7aa83a46122f0c25379b11e923d82501c9eca4e9035637e65a4d7cf36
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51