Current NDC auxiliary source row compounder:569

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: 83826-9018
Product Ndc: 83826-9018
Product Ndc Digits: 838269018
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Timolol, Bimatoprost
Proprietary Name Suffix: [empty]
Nonproprietary Name: Timolol 0.5%, Bimatoprost 0.01%
Dosage Form Name: SOLUTION
Route Name: OPHTHALMIC; TOPICAL
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: OSRX, Inc.
Establishment Name: OSRX, Inc.
Establishment Fei: [empty]
Substance Name: BIMATOPROST; TIMOLOL MALEATE
Active Ingredients Info: .1 mg/1 mL; 5 mg/1 mL
History Active Ingredients Raw: BIMATOPROST; TIMOLOL MALEATE
History Active Ingredients Info Raw: .1 mg/1 mL; 5 mg/1 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 83826-9018-5
Package Ndc: 83826-9018-5
Package Ndc Digits: 8382690185
Package Ndc11: 83826901805
Package Description: 5 mL in 1 BOTTLE, DROPPER (83826-9018-5)
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:569
Source Row Number: 569
Source Row Hash: a999b7ca9745cb11003340fdc3514909616b94a4344362d2e8b18a02354f5896
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "OPHTHALMIC; TOPICAL",
    "PRODUCTNDC": "83826-9018",
    "DEASCHEDULE": "",
    "LABELERNAME": "OSRX, Inc.",
    "SUBSTANCENAME": "BIMATOPROST; TIMOLOL MALEATE",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "83826-9018-5",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Timolol, Bimatoprost",
    "REPORTINGPERIOD": "2025-2",
    "NONPROPRIETARYNAME": "Timolol 0.5%, Bimatoprost 0.01%",
    "PACKAGEDESCRIPTION": "5 mL in 1 BOTTLE, DROPPER (83826-9018-5) ",
    "ACTIVEINGREDIENTSINFO": ".1 mg/1 mL; 5 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:569
Source Row Number: 569
Status Scope: package
Lookup Ndc: 83826-9018-5
Lookup Ndc Digits: 8382690185
Product Ndc: 83826-9018
Product Ndc Digits: 838269018
Package Ndc: 83826-9018-5
Package Ndc Digits: 8382690185
Package Ndc11: 83826901805
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: a999b7ca9745cb11003340fdc3514909616b94a4344362d2e8b18a02354f5896
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51