Current NDC auxiliary source row compounder:87

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: 69194-740
Product Ndc: 69194-740
Product Ndc Digits: 69194740
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: 740 LIDOCAINE HCl 4% BOTTLE
Proprietary Name Suffix: [empty]
Nonproprietary Name: lidocaine HCl
Dosage Form Name: SOLUTION
Route Name: OPHTHALMIC
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: LIDOCAINE HYDROCHLORIDE
Active Ingredients Info: 40 mg/1 mL
History Active Ingredients Raw: LIDOCAINE HYDROCHLORIDE
History Active Ingredients Info Raw: 40 mg/1 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 69194-740-01
Package Ndc: 69194-740-01
Package Ndc Digits: 6919474001
Package Ndc11: 69194074001
Package Description: 3 mL in 1 BOTTLE, DROPPER (69194-740-01)
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:87
Source Row Number: 87
Source Row Hash: 4a3be0bfaf3ade43a6abe13c46583ef98d3d668600233ddcfd2f04c3a253608b
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09

Exact raw FDA source fields#

{
    "ROUTENAME": "OPHTHALMIC",
    "PRODUCTNDC": "69194-740",
    "DEASCHEDULE": "",
    "LABELERNAME": "Pine Pharmaceuticals LLC",
    "SUBSTANCENAME": "LIDOCAINE HYDROCHLORIDE",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "69194-740-01",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "740 LIDOCAINE HCl 4% BOTTLE",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "lidocaine HCl",
    "PACKAGEDESCRIPTION": "3 mL in 1 BOTTLE, DROPPER (69194-740-01) ",
    "ACTIVEINGREDIENTSINFO": "40 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:87
Source Row Number: 87
Status Scope: package
Lookup Ndc: 69194-740-01
Lookup Ndc Digits: 6919474001
Product Ndc: 69194-740
Product Ndc Digits: 69194740
Package Ndc: 69194-740-01
Package Ndc Digits: 6919474001
Package Ndc11: 69194074001
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: 4a3be0bfaf3ade43a6abe13c46583ef98d3d668600233ddcfd2f04c3a253608b
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09