Current NDC auxiliary source row compounder:4115

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: 73693-381
Product Ndc: 73693-381
Product Ndc Digits: 73693381
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: TESTOSTERONE 200 MG
Proprietary Name Suffix: [empty]
Nonproprietary Name: TESTOSTERONE 200 MG
Dosage Form Name: PELLET, IMPLANTABLE
Route Name: SUBCUTANEOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: FARMAKEIO OUTSOURCING LLC
Establishment Name: FARMAKEIO OUTSOURCING LLC
Establishment Fei: [empty]
Substance Name: TESTOSTERONE
Active Ingredients Info: 200 mg
History Active Ingredients Raw: TESTOSTERONE
History Active Ingredients Info Raw: 200 mg
History Dosage Raw: PELLET, IMPLANTABLE
Dea Schedule: CIII
Package Ndc Raw: 73693-381-01
Package Ndc: 73693-381-01
Package Ndc Digits: 7369338101
Package Ndc11: 73693038101
Package Description: 1 PELLET, IMPLANTABLE in 1 POUCH (73693-381-01)
Reporting Period Raw: 2025-2
Reporting Period: 2025-2
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:4115
Source Row Number: 4115
Source Row Hash: 67b9811836acd590926b88e6edff575c573d4e4db09e79848f38cac7142a7c00
Import Run Id: 20261026T055812Z
Loaded At: 2026-10-26 06:02:33

Exact raw FDA source fields#

{
    "ROUTENAME": "SUBCUTANEOUS",
    "PRODUCTNDC": "73693-381",
    "DEASCHEDULE": "CIII",
    "LABELERNAME": "FARMAKEIO OUTSOURCING LLC",
    "SUBSTANCENAME": "TESTOSTERONE",
    "DOSAGEFORMNAME": "PELLET, IMPLANTABLE",
    "NDCPACKAGECODE": "73693-381-01",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "TESTOSTERONE 200 MG",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "TESTOSTERONE 200 MG",
    "PACKAGEDESCRIPTION": "1 PELLET, IMPLANTABLE in 1 POUCH (73693-381-01) ",
    "ACTIVEINGREDIENTSINFO": "200 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:4115
Source Row Number: 4115
Status Scope: package
Lookup Ndc: 73693-381-01
Lookup Ndc Digits: 7369338101
Product Ndc: 73693-381
Product Ndc Digits: 73693381
Package Ndc: 73693-381-01
Package Ndc Digits: 7369338101
Package Ndc11: 73693038101
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2025-2
Reporting Period: 2025-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 67b9811836acd590926b88e6edff575c573d4e4db09e79848f38cac7142a7c00
Import Run Id: 20261026T055812Z
Loaded At: 2026-10-26 06:02:33