Current NDC auxiliary source row compounder:425

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: 81375-002
Product Ndc: 81375-002
Product Ndc Digits: 81375002
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Prednisolone/Bromfenac
Proprietary Name Suffix: [empty]
Nonproprietary Name: Prednisolone 1%//Bromfenac 0.09%
Dosage Form Name: SOLUTION/ DROPS
Route Name: OPHTHALMIC
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: PQ Pharmacy LLC
Establishment Name: PQ Pharmacy LLC
Establishment Fei: [empty]
Substance Name: PREDNISOLONE SODIUM PHOSPHATE; BROMFENAC SODIUM
Active Ingredients Info: 10 mg/1 mL; .9 mg/1 mL
History Active Ingredients Raw: PREDNISOLONE SODIUM PHOSPHATE; BROMFENAC SODIUM
History Active Ingredients Info Raw: 10 mg/1 mL; .9 mg/1 mL
History Dosage Raw: SOLUTION/ DROPS
Dea Schedule: [empty]
Package Ndc Raw: 81375-002-05
Package Ndc: 81375-002-05
Package Ndc Digits: 8137500205
Package Ndc11: 81375000205
Package Description: 5.6 mL in 1 BOTTLE, DROPPER (81375-002-05)
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:425
Source Row Number: 425
Source Row Hash: 10be6e254c8b4427fdd8ddd337f43d689eaccfbd98f3bbb8246ff9d7da0f72f8
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57

Exact raw FDA source fields#

{
    "ROUTENAME": "OPHTHALMIC",
    "PRODUCTNDC": "81375-002",
    "DEASCHEDULE": "",
    "LABELERNAME": "PQ Pharmacy LLC",
    "SUBSTANCENAME": "PREDNISOLONE SODIUM PHOSPHATE; BROMFENAC SODIUM",
    "DOSAGEFORMNAME": "SOLUTION/ DROPS",
    "NDCPACKAGECODE": "81375-002-05",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Prednisolone/Bromfenac",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Prednisolone 1%//Bromfenac 0.09%",
    "PACKAGEDESCRIPTION": "5.6 mL in 1 BOTTLE, DROPPER (81375-002-05) ",
    "ACTIVEINGREDIENTSINFO": "10 mg/1 mL; .9 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:425
Source Row Number: 425
Status Scope: package
Lookup Ndc: 81375-002-05
Lookup Ndc Digits: 8137500205
Product Ndc: 81375-002
Product Ndc Digits: 81375002
Package Ndc: 81375-002-05
Package Ndc Digits: 8137500205
Package Ndc11: 81375000205
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: 10be6e254c8b4427fdd8ddd337f43d689eaccfbd98f3bbb8246ff9d7da0f72f8
Import Run Id: 20261017T224343Z
Loaded At: 2026-10-17 22:48:57