Current NDC auxiliary source row compounder:929
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
- 26436-5526
- Product Ndc
- 26436-5526
- Product Ndc Digits
- 264365526
- Product Type Name
- HUMAN COMPOUNDED DRUG
- Proprietary Name
- Combo Drops
- Proprietary Name Suffix
- Nonproprietary Name
- Cyclopentaloate 2%, Phenyephrine 2.5%, Tropicamide 0.5%
- Dosage Form Name
- SOLUTION/ DROPS
- Route Name
- OPHTHALMIC
- Marketing Category Name
- OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
- Labeler Name
- Hybrid Pharma
- Establishment Name
- Hybrid Pharma
- Establishment Fei
- Substance Name
- PHENYLEPHRINE HYDROCHLORIDE, (+/-)-; TROPICAMIDE; CYCLOPENTOLATE
- Active Ingredients Info
- 25 mg/1 mL; 5 mg/1 mL; 5 mg/1 mL
- History Active Ingredients Raw
- PHENYLEPHRINE HYDROCHLORIDE, (+/-)-; TROPICAMIDE; CYCLOPENTOLATE
- History Active Ingredients Info Raw
- 25 mg/1 mL; 5 mg/1 mL; 5 mg/1 mL
- History Dosage Raw
- SOLUTION/ DROPS
- Dea Schedule
- Package Ndc Raw
- 26436-5526-0
- Package Ndc
- 26436-5526-0
- Package Ndc Digits
- 2643655260
- Package Ndc11
- 26436552600
- Package Description
- 1 mL in 1 BOTTLE, DROPPER (26436-5526-0)
- Reporting Period Raw
- 2026-1
- Reporting Period
- 2026-1
- Normalization Status
- valid
- 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:929
- Source Row Number
- 929
- Source Row Hash
- fad9105cbc4ae8b9320285712eda065844a2f507cad941dc4cf880f9bb3ae6c8
- Import Run Id
- 20261021T042902Z
- Loaded At
- 2026-10-21 04:33:26
Exact raw FDA source fields#
{
"ROUTENAME": "OPHTHALMIC",
"PRODUCTNDC": "26436-5526",
"DEASCHEDULE": "",
"LABELERNAME": "Hybrid Pharma",
"SUBSTANCENAME": "PHENYLEPHRINE HYDROCHLORIDE, (+/-)-; TROPICAMIDE; CYCLOPENTOLATE",
"DOSAGEFORMNAME": "SOLUTION/ DROPS",
"NDCPACKAGECODE": "26436-5526-0",
"PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
"PROPRIETARYNAME": "Combo Drops",
"REPORTINGPERIOD": "2026-1",
"NONPROPRIETARYNAME": "Cyclopentaloate 2%, Phenyephrine 2.5%, Tropicamide 0.5%",
"PACKAGEDESCRIPTION": "1 mL in 1 BOTTLE, DROPPER (26436-5526-0) ",
"ACTIVEINGREDIENTSINFO": "25 mg/1 mL; 5 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:929
- Source Row Number
- 929
- Status Scope
- package
- Lookup Ndc
- 26436-5526-0
- Lookup Ndc Digits
- 2643655260
- Product Ndc
- 26436-5526
- Product Ndc Digits
- 264365526
- Package Ndc
- 26436-5526-0
- Package Ndc Digits
- 2643655260
- Package Ndc11
- 26436552600
- Product Id
- 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
- fad9105cbc4ae8b9320285712eda065844a2f507cad941dc4cf880f9bb3ae6c8
- Import Run Id
- 20261021T042902Z
- Loaded At
- 2026-10-21 04:33:26