Current NDC auxiliary source row compounder:482
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
- 71285-0203
- Product Ndc
- 71285-0203
- Product Ndc Digits
- 712850203
- Product Type Name
- HUMAN COMPOUNDED DRUG
- Proprietary Name
- Modified St. Thomas Low K (62 mEq) High Sodium Bicarbonate 1000 mL Bag
- Proprietary Name Suffix
- Nonproprietary Name
- Modified St. Thomas Low K (62 mEq) High Sodium Bicarbonate 1000 mL Bag
- Dosage Form Name
- SOLUTION
- Route Name
- INTRACORONARY
- Marketing Category Name
- OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
- Labeler Name
- Central Admixture Pharmacy Services, Inc.
- Establishment Name
- Central Admixture Pharmacy Services, Inc.
- Establishment Fei
- Substance Name
- SODIUM CHLORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; CALCIUM CHLORIDE
- Active Ingredients Info
- 100 meq/1000 mL; 29.232 meq/1000 mL; 62 meq/1000 mL; 3.864 g/1000 mL; 2.176 meq/1000 mL
- History Active Ingredients Raw
- SODIUM CHLORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; CALCIUM CHLORIDE
- History Active Ingredients Info Raw
- 100 meq/1000 mL; 29.232 meq/1000 mL; 62 meq/1000 mL; 3.864 g/1000 mL; 2.176 meq/1000 mL
- History Dosage Raw
- SOLUTION
- Dea Schedule
- Package Ndc Raw
- 71285-0203-1
- Package Ndc
- 71285-0203-1
- Package Ndc Digits
- 7128502031
- Package Ndc11
- 71285020301
- Package Description
- 1052.8 mL in 1 BAG (71285-0203-1)
- 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:482
- Source Row Number
- 482
- Source Row Hash
- e0fd1be34afb8f73475c25b39b88da51c7cddb9edd7716a9b43def681e608828
- Import Run Id
- 20261015T162751Z
- Loaded At
- 2026-10-15 16:32:20
Exact raw FDA source fields#
{
"ROUTENAME": "INTRACORONARY",
"PRODUCTNDC": "71285-0203",
"DEASCHEDULE": "",
"LABELERNAME": "Central Admixture Pharmacy Services, Inc.",
"SUBSTANCENAME": "SODIUM CHLORIDE; MAGNESIUM SULFATE HEPTAHYDRATE; POTASSIUM CHLORIDE; SODIUM BICARBONATE; CALCIUM CHLORIDE",
"DOSAGEFORMNAME": "SOLUTION",
"NDCPACKAGECODE": "71285-0203-1",
"PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
"PROPRIETARYNAME": "Modified St. Thomas Low K (62 mEq) High Sodium Bicarbonate 1000 mL Bag",
"REPORTINGPERIOD": "2026-1",
"NONPROPRIETARYNAME": "Modified St. Thomas Low K (62 mEq) High Sodium Bicarbonate 1000 mL Bag",
"PACKAGEDESCRIPTION": "1052.8 mL in 1 BAG (71285-0203-1) ",
"ACTIVEINGREDIENTSINFO": "100 meq/1000 mL; 29.232 meq/1000 mL; 62 meq/1000 mL; 3.864 g/1000 mL; 2.176 meq/1000 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:482
- Source Row Number
- 482
- Status Scope
- package
- Lookup Ndc
- 71285-0203-1
- Lookup Ndc Digits
- 7128502031
- Product Ndc
- 71285-0203
- Product Ndc Digits
- 712850203
- Package Ndc
- 71285-0203-1
- Package Ndc Digits
- 7128502031
- Package Ndc11
- 71285020301
- 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
- e0fd1be34afb8f73475c25b39b88da51c7cddb9edd7716a9b43def681e608828
- Import Run Id
- 20261015T162751Z
- Loaded At
- 2026-10-15 16:32:20