Current NDC auxiliary source row compounder:18

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: 63037-117
Product Ndc: 63037-117
Product Ndc Digits: 63037117
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Diltiazem HCl
Proprietary Name Suffix: [empty]
Nonproprietary Name: Diltiazem HCl
Dosage Form Name: INJECTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Hikma Injectables USA Inc.
Establishment Name: Hikma Injectables USA Inc.
Establishment Fei: [empty]
Substance Name: DILTIAZEM HYDROCHLORIDE
Active Ingredients Info: 125 mg/125 mL
History Active Ingredients Raw: DILTIAZEM HYDROCHLORIDE
History Active Ingredients Info Raw: 125 mg/125 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 63037-117-05
Package Ndc: 63037-117-05
Package Ndc Digits: 6303711705
Package Ndc11: 63037011705
Package Description: 125 mL in 1 BAG (63037-117-05)
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:18
Source Row Number: 18
Source Row Hash: b212c7e204f13e03c19673843afa31f9a0a8cbbe8e1a5d274441fcf9b60782d2
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "63037-117",
    "DEASCHEDULE": "",
    "LABELERNAME": "Hikma Injectables USA Inc.",
    "SUBSTANCENAME": "DILTIAZEM HYDROCHLORIDE",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "63037-117-05",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Diltiazem HCl",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Diltiazem HCl",
    "PACKAGEDESCRIPTION": "125 mL in 1 BAG (63037-117-05) ",
    "ACTIVEINGREDIENTSINFO": "125 mg/125 mL",
    "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:18
Source Row Number: 18
Status Scope: package
Lookup Ndc: 63037-117-05
Lookup Ndc Digits: 6303711705
Product Ndc: 63037-117
Product Ndc Digits: 63037117
Package Ndc: 63037-117-05
Package Ndc Digits: 6303711705
Package Ndc11: 63037011705
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: b212c7e204f13e03c19673843afa31f9a0a8cbbe8e1a5d274441fcf9b60782d2
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20