Current NDC auxiliary source row compounder:3213

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: 72682-8012
Product Ndc: 72682-8012
Product Ndc Digits: 726828012
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Testosterone 12.5mg Pellet
Proprietary Name Suffix: [empty]
Nonproprietary Name: Testosterone 12.5mg Pellet
Dosage Form Name: PELLET
Route Name: SUBCUTANEOUS
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: TESTOSTERONE
Active Ingredients Info: 12.5 mg/12.5 mg
History Active Ingredients Raw: TESTOSTERONE
History Active Ingredients Info Raw: 12.5 mg/12.5 mg
History Dosage Raw: PELLET
Dea Schedule: CIII
Package Ndc Raw: 72682-8012-1
Package Ndc: 72682-8012-1
Package Ndc Digits: 7268280121
Package Ndc11: 72682801201
Package Description: 1 mg in 1 VIAL (72682-8012-1)
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:3213
Source Row Number: 3213
Source Row Hash: 4d53cdd65789e6c3a7f6c85103124945d86ba3f9525cb37212b742666179a05a
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01

Exact raw FDA source fields#

{
    "ROUTENAME": "SUBCUTANEOUS",
    "PRODUCTNDC": "72682-8012",
    "DEASCHEDULE": "CIII",
    "LABELERNAME": "AnazaoHealth Corporation",
    "SUBSTANCENAME": "TESTOSTERONE",
    "DOSAGEFORMNAME": "PELLET",
    "NDCPACKAGECODE": "72682-8012-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Testosterone 12.5mg Pellet",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "Testosterone 12.5mg Pellet",
    "PACKAGEDESCRIPTION": "1 mg in 1 VIAL (72682-8012-1) ",
    "ACTIVEINGREDIENTSINFO": "12.5 mg/12.5 mg",
    "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:3213
Source Row Number: 3213
Status Scope: package
Lookup Ndc: 72682-8012-1
Lookup Ndc Digits: 7268280121
Product Ndc: 72682-8012
Product Ndc Digits: 726828012
Package Ndc: 72682-8012-1
Package Ndc Digits: 7268280121
Package Ndc11: 72682801201
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: 4d53cdd65789e6c3a7f6c85103124945d86ba3f9525cb37212b742666179a05a
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01