Current NDC auxiliary source row compounder:775

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: 69374-982
Product Ndc: 69374-982
Product Ndc Digits: 69374982
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Ketamine Hydrochloride 30 mg/3 mL
Proprietary Name Suffix: [empty]
Nonproprietary Name: Ketamine HCL 30 mg/3 mL
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRAMUSCULAR; INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Nephron Sterile Compounding Center, LLC
Establishment Name: Nephron Sterile Compounding Center, LLC
Establishment Fei: [empty]
Substance Name: KETAMINE HYDROCHLORIDE
Active Ingredients Info: 30 mg/3 mL
History Active Ingredients Raw: KETAMINE HYDROCHLORIDE
History Active Ingredients Info Raw: 30 mg/3 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: CIII
Package Ndc Raw: 69374-982-55
Package Ndc: 69374-982-55
Package Ndc Digits: 6937498255
Package Ndc11: 69374098255
Package Description: 6 CARTON in 1 CASE (69374-982-55) > 5 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
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:775
Source Row Number: 775
Source Row Hash: 1ba1989054ab592f4479c594d4de8ea915440f1d84a6a79d47ee880bc40cdf32
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAMUSCULAR; INTRAVENOUS",
    "PRODUCTNDC": "69374-982",
    "DEASCHEDULE": "CIII",
    "LABELERNAME": "Nephron Sterile Compounding Center, LLC",
    "SUBSTANCENAME": "KETAMINE HYDROCHLORIDE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "69374-982-55",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Ketamine Hydrochloride 30 mg/3 mL",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "Ketamine HCL 30 mg/3 mL",
    "PACKAGEDESCRIPTION": "6 CARTON in 1 CASE (69374-982-55)  > 5 SYRINGE, PLASTIC in 1 CARTON > 5 mL in 1 SYRINGE, PLASTIC",
    "ACTIVEINGREDIENTSINFO": "30 mg/3 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:775
Source Row Number: 775
Status Scope: package
Lookup Ndc: 69374-982-55
Lookup Ndc Digits: 6937498255
Product Ndc: 69374-982
Product Ndc Digits: 69374982
Package Ndc: 69374-982-55
Package Ndc Digits: 6937498255
Package Ndc11: 69374098255
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 1ba1989054ab592f4479c594d4de8ea915440f1d84a6a79d47ee880bc40cdf32
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51