← Current compounder rows

Current NDC auxiliary source row compounder:56

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
72682-8214
Product Ndc
72682-8214
Product Ndc Digits
726828214
Product Type Name
HUMAN COMPOUNDED DRUG
Proprietary Name
Testosterone 100mg/Anastrozole 4mg Pellet
Proprietary Name Suffix
[empty]
Nonproprietary Name
Testosterone 100mg/Anastrozole 4mg 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
ANASTROZOLE; TESTOSTERONE
Active Ingredients Info
1 mg/1 mg; 1 mg/1 mg
History Active Ingredients Raw
ANASTROZOLE; TESTOSTERONE
History Active Ingredients Info Raw
1 mg/1 mg; 1 mg/1 mg
History Dosage Raw
PELLET
Dea Schedule
CIII
Package Ndc Raw
72682-8214-1
Package Ndc
72682-8214-1
Package Ndc Digits
7268282141
Package Ndc11
72682821401
Package Description
1 mg in 1 VIAL (72682-8214-1)
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:56
Source Row Number
56
Source Row Hash
42ca7a1a864957a13a8f790b5fded622c64d9e1a90aba50a139210870764a9ea
Import Run Id
20261015T162751Z
Loaded At
2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "SUBCUTANEOUS",
    "PRODUCTNDC": "72682-8214",
    "DEASCHEDULE": "CIII",
    "LABELERNAME": "AnazaoHealth Corporation",
    "SUBSTANCENAME": "ANASTROZOLE; TESTOSTERONE",
    "DOSAGEFORMNAME": "PELLET",
    "NDCPACKAGECODE": "72682-8214-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Testosterone 100mg/Anastrozole 4mg Pellet",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Testosterone 100mg/Anastrozole 4mg Pellet",
    "PACKAGEDESCRIPTION": "1 mg in 1 VIAL (72682-8214-1) ",
    "ACTIVEINGREDIENTSINFO": "1 mg/1 mg; 1 mg/1 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:56
Source Row Number
56
Status Scope
package
Lookup Ndc
72682-8214-1
Lookup Ndc Digits
7268282141
Product Ndc
72682-8214
Product Ndc Digits
726828214
Package Ndc
72682-8214-1
Package Ndc Digits
7268282141
Package Ndc11
72682821401
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
42ca7a1a864957a13a8f790b5fded622c64d9e1a90aba50a139210870764a9ea
Import Run Id
20261015T162751Z
Loaded At
2026-10-15 16:32:20