Current NDC auxiliary source row compounder:67

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: 71449-089
Product Ndc: 71449-089
Product Ndc Digits: 71449089
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Moxifloxacin
Proprietary Name Suffix: Preservative Free
Nonproprietary Name: Moxifloxacin
Dosage Form Name: INJECTION, SOLUTION
Route Name: INTRAOCULAR
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Denver Solutions, LLC dba Leiters Health
Establishment Name: Denver Solutions, LLC dba Leiters Health
Establishment Fei: [empty]
Substance Name: MOXIFLOXACIN HYDROCHLORIDE
Active Ingredients Info: 1 mg/1 mL
History Active Ingredients Raw: MOXIFLOXACIN HYDROCHLORIDE
History Active Ingredients Info Raw: 1 mg/1 mL
History Dosage Raw: INJECTION, SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 71449-089-42
Package Ndc: 71449-089-42
Package Ndc Digits: 7144908942
Package Ndc11: 71449008942
Package Description: 10 VIAL, SINGLE-USE in 1 BOX (71449-089-42) > 1 mL in 1 VIAL, SINGLE-USE
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
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:67
Source Row Number: 67
Source Row Hash: f25ea9d274f0f5359beb4ff91dc80a5b767278a55cef2c03955e7e7cc32210ed
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAOCULAR",
    "PRODUCTNDC": "71449-089",
    "DEASCHEDULE": "",
    "LABELERNAME": "Denver Solutions, LLC dba Leiters Health",
    "SUBSTANCENAME": "MOXIFLOXACIN HYDROCHLORIDE",
    "DOSAGEFORMNAME": "INJECTION, SOLUTION",
    "NDCPACKAGECODE": "71449-089-42",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Moxifloxacin",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Moxifloxacin",
    "PACKAGEDESCRIPTION": "10 VIAL, SINGLE-USE in 1 BOX (71449-089-42)  > 1 mL in 1 VIAL, SINGLE-USE",
    "ACTIVEINGREDIENTSINFO": "1 mg/1 mL",
    "MARKETINGCATEGORYNAME": "OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)",
    "PROPRIETARYNAMESUFFIX": "Preservative Free"
}

Normalization notes#

[]

Current status projection#

Dataset: compounder
Record Source: ndc_compounder_zip
Source Record Id: compounder:67
Source Row Number: 67
Status Scope: package
Lookup Ndc: 71449-089-42
Lookup Ndc Digits: 7144908942
Product Ndc: 71449-089
Product Ndc Digits: 71449089
Package Ndc: 71449-089-42
Package Ndc Digits: 7144908942
Package Ndc11: 71449008942
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: f25ea9d274f0f5359beb4ff91dc80a5b767278a55cef2c03955e7e7cc32210ed
Import Run Id: 20261013T114159Z
Loaded At: 2026-10-13 11:48:09