Current NDC auxiliary source row compounder:3787

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: 26436-5644
Product Ndc: 26436-5644
Product Ndc Digits: 264365644
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: PROGESTERONE
Proprietary Name Suffix: [empty]
Nonproprietary Name: PROGESTERONE
Dosage Form Name: SUPPOSITORY
Route Name: VAGINAL
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Hybrid Pharma
Establishment Name: Hybrid Pharma
Establishment Fei: [empty]
Substance Name: PROGESTERONE
Active Ingredients Info: 100 mg
History Active Ingredients Raw: PROGESTERONE
History Active Ingredients Info Raw: 100 mg
History Dosage Raw: SUPPOSITORY
Dea Schedule: [empty]
Package Ndc Raw: 26436-5644-1
Package Ndc: 26436-5644-1
Package Ndc Digits: 2643656441
Package Ndc11: 26436564401
Package Description: 1 SUPPOSITORY in 1 CONTAINER (26436-5644-1)
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:3787
Source Row Number: 3787
Source Row Hash: 22e515997092e3055a396e920815e1eb395e8eaa6bd0c7ab7d3bc25dc89eb162
Import Run Id: 20261026T055812Z
Loaded At: 2026-10-26 06:02:33

Exact raw FDA source fields#

{
    "ROUTENAME": "VAGINAL",
    "PRODUCTNDC": "26436-5644",
    "DEASCHEDULE": "",
    "LABELERNAME": "Hybrid Pharma",
    "SUBSTANCENAME": "PROGESTERONE",
    "DOSAGEFORMNAME": "SUPPOSITORY",
    "NDCPACKAGECODE": "26436-5644-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "PROGESTERONE",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "PROGESTERONE",
    "PACKAGEDESCRIPTION": "1 SUPPOSITORY in 1 CONTAINER (26436-5644-1) ",
    "ACTIVEINGREDIENTSINFO": "100 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:3787
Source Row Number: 3787
Status Scope: package
Lookup Ndc: 26436-5644-1
Lookup Ndc Digits: 2643656441
Product Ndc: 26436-5644
Product Ndc Digits: 264365644
Package Ndc: 26436-5644-1
Package Ndc Digits: 2643656441
Package Ndc11: 26436564401
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: 22e515997092e3055a396e920815e1eb395e8eaa6bd0c7ab7d3bc25dc89eb162
Import Run Id: 20261026T055812Z
Loaded At: 2026-10-26 06:02:33