Current NDC auxiliary source row compounder:124
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
- 73198-104
- Product Ndc
- 73198-104
- Product Ndc Digits
- 73198104
- Product Type Name
- HUMAN COMPOUNDED DRUG
- Proprietary Name
- Tri-Immune Boost
- Proprietary Name Suffix
- Nonproprietary Name
- Glutathione 200 mg/mL Ascorbic Acid 200 mg/mL Zinc Sulfate Heptahydrate 2.5 mg/mL
- Dosage Form Name
- INJECTION, SOLUTION
- Route Name
- INTRAMUSCULAR; INTRAVENOUS
- Marketing Category Name
- OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
- Labeler Name
- Olympia Pharmacy
- Establishment Name
- Olympia Pharmacy
- Establishment Fei
- Substance Name
- GLUTATHIONE; ASCORBIC ACID; ZINC SULFATE HEPTAHYDRATE
- Active Ingredients Info
- 200 mg/1 mL; 200 mg/1 mL; .5686 mg/1 mL
- History Active Ingredients Raw
- GLUTATHIONE; ASCORBIC ACID; ZINC SULFATE HEPTAHYDRATE
- History Active Ingredients Info Raw
- 200 mg/1 mL; 200 mg/1 mL; .5686 mg/1 mL
- History Dosage Raw
- INJECTION, SOLUTION
- Dea Schedule
- Package Ndc Raw
- 73198-104-30
- Package Ndc
- 73198-104-30
- Package Ndc Digits
- 7319810430
- Package Ndc11
- 73198010430
- Package Description
- 30 mL in 1 VIAL, MULTI-DOSE (73198-104-30)
- 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:124
- Source Row Number
- 124
- Source Row Hash
- fcd054606dfeab7ab645efcdb5ae9d199f760833ab3cbbb469d2b00cce9560cc
- Import Run Id
- 20261015T162751Z
- Loaded At
- 2026-10-15 16:32:20
Exact raw FDA source fields#
{
"ROUTENAME": "INTRAMUSCULAR; INTRAVENOUS",
"PRODUCTNDC": "73198-104",
"DEASCHEDULE": "",
"LABELERNAME": "Olympia Pharmacy",
"SUBSTANCENAME": "GLUTATHIONE; ASCORBIC ACID; ZINC SULFATE HEPTAHYDRATE",
"DOSAGEFORMNAME": "INJECTION, SOLUTION",
"NDCPACKAGECODE": "73198-104-30",
"PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
"PROPRIETARYNAME": "Tri-Immune Boost",
"REPORTINGPERIOD": "2026-1",
"NONPROPRIETARYNAME": "Glutathione 200 mg/mL Ascorbic Acid 200 mg/mL Zinc Sulfate Heptahydrate 2.5 mg/mL",
"PACKAGEDESCRIPTION": "30 mL in 1 VIAL, MULTI-DOSE (73198-104-30) ",
"ACTIVEINGREDIENTSINFO": "200 mg/1 mL; 200 mg/1 mL; .5686 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:124
- Source Row Number
- 124
- Status Scope
- package
- Lookup Ndc
- 73198-104-30
- Lookup Ndc Digits
- 7319810430
- Product Ndc
- 73198-104
- Product Ndc Digits
- 73198104
- Package Ndc
- 73198-104-30
- Package Ndc Digits
- 7319810430
- Package Ndc11
- 73198010430
- 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
- fcd054606dfeab7ab645efcdb5ae9d199f760833ab3cbbb469d2b00cce9560cc
- Import Run Id
- 20261015T162751Z
- Loaded At
- 2026-10-15 16:32:20