Current NDC auxiliary source row compounder:1071

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: 61141-1318
Product Ndc: 61141-1318
Product Ndc Digits: 611411318
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Fentanyl Citrate 2500mcg/250mL (10mcg/mL) bag
Proprietary Name Suffix: [empty]
Nonproprietary Name: Fentanyl Citrate Drip
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Medi-Fare Drug
Establishment Name: Medi-Fare Drug
Establishment Fei: [empty]
Substance Name: FENTANYL CITRATE
Active Ingredients Info: 10 ug/1 mL
History Active Ingredients Raw: FENTANYL CITRATE
History Active Ingredients Info Raw: 10 ug/1 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: CII
Package Ndc Raw: 61141-1318-1
Package Ndc: 61141-1318-1
Package Ndc Digits: 6114113181
Package Ndc11: 61141131801
Package Description: 250 mL in 1 BAG (61141-1318-1)
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:1071
Source Row Number: 1071
Source Row Hash: e45831437485d7844278394c146465e871a51e30dfd5db0256e1f62dcfc3fa41
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "61141-1318",
    "DEASCHEDULE": "CII",
    "LABELERNAME": "Medi-Fare Drug",
    "SUBSTANCENAME": "FENTANYL CITRATE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "61141-1318-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Fentanyl Citrate 2500mcg/250mL (10mcg/mL) bag",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "Fentanyl Citrate Drip",
    "PACKAGEDESCRIPTION": "250 mL in 1 BAG (61141-1318-1) ",
    "ACTIVEINGREDIENTSINFO": "10 ug/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:1071
Source Row Number: 1071
Status Scope: package
Lookup Ndc: 61141-1318-1
Lookup Ndc Digits: 6114113181
Product Ndc: 61141-1318
Product Ndc Digits: 611411318
Package Ndc: 61141-1318-1
Package Ndc Digits: 6114113181
Package Ndc11: 61141131801
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: e45831437485d7844278394c146465e871a51e30dfd5db0256e1f62dcfc3fa41
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51