Current NDC auxiliary source row compounder:2102

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: 69194-555
Product Ndc: 69194-555
Product Ndc Digits: 69194555
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: 555 CEFUROXIME 10MG/ML SYRINGE
Proprietary Name Suffix: [empty]
Nonproprietary Name: cefuroxime
Dosage Form Name: INJECTION
Route Name: INTRAOCULAR
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Pine Pharmaceuticals LLC
Establishment Name: Pine Pharmaceuticals LLC
Establishment Fei: [empty]
Substance Name: CEFUROXIME SODIUM
Active Ingredients Info: 1 mg/.1 mL
History Active Ingredients Raw: CEFUROXIME SODIUM
History Active Ingredients Info Raw: 1 mg/.1 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 69194-555-01
Package Ndc: 69194-555-01
Package Ndc Digits: 6919455501
Package Ndc11: 69194055501
Package Description: .4 mL in 1 SYRINGE (69194-555-01)
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:2102
Source Row Number: 2102
Source Row Hash: afdc4e831ad219f0249c437975116b03879f7c3d0e817770b96dd263323ac79b
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAOCULAR",
    "PRODUCTNDC": "69194-555",
    "DEASCHEDULE": "",
    "LABELERNAME": "Pine Pharmaceuticals LLC",
    "SUBSTANCENAME": "CEFUROXIME SODIUM",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "69194-555-01",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "555 CEFUROXIME 10MG/ML SYRINGE",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "cefuroxime",
    "PACKAGEDESCRIPTION": ".4 mL in 1 SYRINGE (69194-555-01) ",
    "ACTIVEINGREDIENTSINFO": "1 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:2102
Source Row Number: 2102
Status Scope: package
Lookup Ndc: 69194-555-01
Lookup Ndc Digits: 6919455501
Product Ndc: 69194-555
Product Ndc Digits: 69194555
Package Ndc: 69194-555-01
Package Ndc Digits: 6919455501
Package Ndc11: 69194055501
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: afdc4e831ad219f0249c437975116b03879f7c3d0e817770b96dd263323ac79b
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01