Current NDC auxiliary source row compounder:1111

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: 83863-9010
Product Ndc: 83863-9010
Product Ndc Digits: 838639010
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Fentanyl citrate 10 mcg in NS 1 mL Syringe
Proprietary Name Suffix: [empty]
Nonproprietary Name: Fentanyl citrate 10 mcg in NS 1 mL Syringe
Dosage Form Name: INJECTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Park Avenue Compounding
Establishment Name: Park Avenue Compounding
Establishment Fei: [empty]
Substance Name: FENTANYL CITRATE
Active Ingredients Info: .01 mg/1 mL
History Active Ingredients Raw: FENTANYL CITRATE
History Active Ingredients Info Raw: .01 mg/1 mL
History Dosage Raw: INJECTION
Dea Schedule: CII
Package Ndc Raw: 83863-9010-2
Package Ndc: 83863-9010-2
Package Ndc Digits: 8386390102
Package Ndc11: 83863901002
Package Description: 1 mL in 1 SYRINGE, PLASTIC (83863-9010-2)
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:1111
Source Row Number: 1111
Source Row Hash: 469a812f0b95b80d9b176e67f22348d3cb25864c45dc471ec37ac9433a0ce4d9
Import Run Id: 20261020T231736Z
Loaded At: 2026-10-20 23:22:14

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "83863-9010",
    "DEASCHEDULE": "CII",
    "LABELERNAME": "Park Avenue Compounding",
    "SUBSTANCENAME": "FENTANYL CITRATE",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "83863-9010-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Fentanyl citrate 10 mcg in NS 1 mL Syringe",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "Fentanyl citrate 10 mcg in NS 1 mL Syringe",
    "PACKAGEDESCRIPTION": "1 mL in 1 SYRINGE, PLASTIC (83863-9010-2) ",
    "ACTIVEINGREDIENTSINFO": ".01 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:1111
Source Row Number: 1111
Status Scope: package
Lookup Ndc: 83863-9010-2
Lookup Ndc Digits: 8386390102
Product Ndc: 83863-9010
Product Ndc Digits: 838639010
Package Ndc: 83863-9010-2
Package Ndc Digits: 8386390102
Package Ndc11: 83863901002
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: 469a812f0b95b80d9b176e67f22348d3cb25864c45dc471ec37ac9433a0ce4d9
Import Run Id: 20261020T231736Z
Loaded At: 2026-10-20 23:22:14