Current NDC auxiliary source row compounder:4232

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: 73013-2002
Product Ndc: 73013-2002
Product Ndc Digits: 730132002
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Ketamine Hydrochloride 10mg/mL
Proprietary Name Suffix: [empty]
Nonproprietary Name: Ketamine HCl
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRAMUSCULAR; INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: OurPharma LLC
Establishment Name: OurPharma LLC
Establishment Fei: [empty]
Substance Name: KETAMINE HYDROCHLORIDE
Active Ingredients Info: 10 mg/1 mL
History Active Ingredients Raw: KETAMINE HYDROCHLORIDE
History Active Ingredients Info Raw: 10 mg/1 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: CIII
Package Ndc Raw: 73013-2002-2
Package Ndc: 73013-2002-2
Package Ndc Digits: 7301320022
Package Ndc11: 73013200202
Package Description: 5 mL in 1 SYRINGE (73013-2002-2)
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:4232
Source Row Number: 4232
Source Row Hash: b03854efb2f3e2e8db8d73bdc7800025730b5d0aa33448fc128678db592c4085
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAMUSCULAR; INTRAVENOUS",
    "PRODUCTNDC": "73013-2002",
    "DEASCHEDULE": "CIII",
    "LABELERNAME": "OurPharma LLC",
    "SUBSTANCENAME": "KETAMINE HYDROCHLORIDE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "73013-2002-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Ketamine Hydrochloride 10mg/mL",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Ketamine HCl",
    "PACKAGEDESCRIPTION": "5 mL in 1 SYRINGE (73013-2002-2) ",
    "ACTIVEINGREDIENTSINFO": "10 mg/1 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:4232
Source Row Number: 4232
Status Scope: package
Lookup Ndc: 73013-2002-2
Lookup Ndc Digits: 7301320022
Product Ndc: 73013-2002
Product Ndc Digits: 730132002
Package Ndc: 73013-2002-2
Package Ndc Digits: 7301320022
Package Ndc11: 73013200202
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: b03854efb2f3e2e8db8d73bdc7800025730b5d0aa33448fc128678db592c4085
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27