Current NDC auxiliary source row compounder:450

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: 26436-5628
Product Ndc: 26436-5628
Product Ndc Digits: 264365628
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: DILTIAZEM 2%
Proprietary Name Suffix: [empty]
Nonproprietary Name: DILTIAZEM 2%
Dosage Form Name: OINTMENT
Route Name: TOPICAL
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: DILTIAZEM HCL
Active Ingredients Info: 20 mg/1 g
History Active Ingredients Raw: DILTIAZEM HCL
History Active Ingredients Info Raw: 20 mg/1 g
History Dosage Raw: OINTMENT
Dea Schedule: [empty]
Package Ndc Raw: 26436-5628-3
Package Ndc: 26436-5628-3
Package Ndc Digits: 2643656283
Package Ndc11: 26436562803
Package Description: 30 g in 1 JAR (26436-5628-3)
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
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:450
Source Row Number: 450
Source Row Hash: bc7cd967142808b2ed66e56ae381439b32ce5d7d0ccfdfaead1fcec394bfa3f4
Import Run Id: 20261021T042902Z
Loaded At: 2026-10-21 04:33:26

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "26436-5628",
    "DEASCHEDULE": "",
    "LABELERNAME": "Hybrid Pharma",
    "SUBSTANCENAME": "DILTIAZEM HCL",
    "DOSAGEFORMNAME": "OINTMENT",
    "NDCPACKAGECODE": "26436-5628-3",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "DILTIAZEM 2%",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "DILTIAZEM 2%",
    "PACKAGEDESCRIPTION": "30 g in 1 JAR (26436-5628-3) ",
    "ACTIVEINGREDIENTSINFO": "20 mg/1 g",
    "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:450
Source Row Number: 450
Status Scope: package
Lookup Ndc: 26436-5628-3
Lookup Ndc Digits: 2643656283
Product Ndc: 26436-5628
Product Ndc Digits: 264365628
Package Ndc: 26436-5628-3
Package Ndc Digits: 2643656283
Package Ndc11: 26436562803
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: bc7cd967142808b2ed66e56ae381439b32ce5d7d0ccfdfaead1fcec394bfa3f4
Import Run Id: 20261021T042902Z
Loaded At: 2026-10-21 04:33:26