Current NDC auxiliary source row compounder:494
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
- 71285-8100
- Product Ndc
- 71285-8100
- Product Ndc Digits
- 712858100
- Product Type Name
- HUMAN COMPOUNDED DRUG
- Proprietary Name
- Heparin 2500units added to NS
- Proprietary Name Suffix
- Nonproprietary Name
- Heparin 2500units added to NS
- Dosage Form Name
- SOLUTION
- Route Name
- INTRAVENOUS
- 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
- HEPARIN SODIUM
- Active Ingredients Info
- 2500 U/500 mL
- History Active Ingredients Raw
- HEPARIN SODIUM
- History Active Ingredients Info Raw
- 2500 U/500 mL
- History Dosage Raw
- SOLUTION
- Dea Schedule
- Package Ndc Raw
- 71285-8100-1
- Package Ndc
- 71285-8100-1
- Package Ndc Digits
- 7128581001
- Package Ndc11
- 71285810001
- Package Description
- 500 mL in 1 BAG (71285-8100-1)
- Reporting Period Raw
- 2025-2
- Reporting Period
- 2025-2
- 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:494
- Source Row Number
- 494
- Source Row Hash
- b4ba4893245cc85d247607a75618668f6e0f2022cff621891fa61723a3e400ff
- Import Run Id
- 20261017T224343Z
- Loaded At
- 2026-10-17 22:48:57
Exact raw FDA source fields#
{
"ROUTENAME": "INTRAVENOUS",
"PRODUCTNDC": "71285-8100",
"DEASCHEDULE": "",
"LABELERNAME": "Central Admixture Pharmacy Services, Inc.",
"SUBSTANCENAME": "HEPARIN SODIUM",
"DOSAGEFORMNAME": "SOLUTION",
"NDCPACKAGECODE": "71285-8100-1",
"PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
"PROPRIETARYNAME": "Heparin 2500units added to NS",
"REPORTINGPERIOD": "2025-2",
"NONPROPRIETARYNAME": "Heparin 2500units added to NS",
"PACKAGEDESCRIPTION": "500 mL in 1 BAG (71285-8100-1) ",
"ACTIVEINGREDIENTSINFO": "2500 U/500 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:494
- Source Row Number
- 494
- Status Scope
- package
- Lookup Ndc
- 71285-8100-1
- Lookup Ndc Digits
- 7128581001
- Product Ndc
- 71285-8100
- Product Ndc Digits
- 712858100
- Package Ndc
- 71285-8100-1
- Package Ndc Digits
- 7128581001
- Package Ndc11
- 71285810001
- Product Id
- 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
- b4ba4893245cc85d247607a75618668f6e0f2022cff621891fa61723a3e400ff
- Import Run Id
- 20261017T224343Z
- Loaded At
- 2026-10-17 22:48:57