Current NDC auxiliary source row compounder:3206

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: 71285-0101
Product Ndc: 71285-0101
Product Ndc Digits: 712850101
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Induction 4 to1 High K (36mEq) Low Tromethamine 500ml Bag
Proprietary Name Suffix: [empty]
Nonproprietary Name: Induction 4 to1 High K (36mEq) Low Tromethamine 500ml 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: [empty]
Substance Name: SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ANHYDROUS DEXTROSE; CITRIC ACID MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE; SODIUM CHLORIDE; TROMETHAMINE; POTASSIUM CHLORIDE; DEXTROSE MONOHYDRATE
Active Ingredients Info: .666 g/500 mL; 13.92 g/500 mL; .981 g/500 mL; 7.89 g/500 mL; 13.6 meq/500 mL; 2.16 g/500 mL; 36 meq/500 mL; 19.6 g/500 mL
History Active Ingredients Raw: SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ANHYDROUS DEXTROSE; CITRIC ACID MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE; SODIUM CHLORIDE; TROMETHAMINE; POTASSIUM CHLORIDE; DEXTROSE MONOHYDRATE
History Active Ingredients Info Raw: .666 g/500 mL; 13.92 g/500 mL; .981 g/500 mL; 7.89 g/500 mL; 13.6 meq/500 mL; 2.16 g/500 mL; 36 meq/500 mL; 19.6 g/500 mL
History Dosage Raw: SOLUTION
Dea Schedule: [empty]
Package Ndc Raw: 71285-0101-1
Package Ndc: 71285-0101-1
Package Ndc Digits: 7128501011
Package Ndc11: 71285010101
Package Description: 500 mL in 1 BAG (71285-0101-1)
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
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:3206
Source Row Number: 3206
Source Row Hash: 73f4a8353d884a235c9987f190f0fa6418111b3de2cc5b0a2855182a703c1db3
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRACORONARY",
    "PRODUCTNDC": "71285-0101",
    "DEASCHEDULE": "",
    "LABELERNAME": "Central Admixture Pharmacy Services, Inc.",
    "SUBSTANCENAME": "SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE; ANHYDROUS DEXTROSE; CITRIC ACID MONOHYDRATE; TRISODIUM CITRATE DIHYDRATE; SODIUM CHLORIDE; TROMETHAMINE; POTASSIUM CHLORIDE; DEXTROSE MONOHYDRATE",
    "DOSAGEFORMNAME": "SOLUTION",
    "NDCPACKAGECODE": "71285-0101-1",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Induction 4 to1 High K (36mEq) Low Tromethamine 500ml Bag",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Induction 4 to1 High K (36mEq) Low Tromethamine 500ml Bag",
    "PACKAGEDESCRIPTION": "500 mL in 1 BAG (71285-0101-1) ",
    "ACTIVEINGREDIENTSINFO": ".666 g/500 mL; 13.92 g/500 mL; .981 g/500 mL; 7.89 g/500 mL; 13.6 meq/500 mL; 2.16 g/500 mL; 36 meq/500 mL; 19.6 g/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:3206
Source Row Number: 3206
Status Scope: package
Lookup Ndc: 71285-0101-1
Lookup Ndc Digits: 7128501011
Product Ndc: 71285-0101
Product Ndc Digits: 712850101
Package Ndc: 71285-0101-1
Package Ndc Digits: 7128501011
Package Ndc11: 71285010101
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2025-1
Reporting Period: 2025-1
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 73f4a8353d884a235c9987f190f0fa6418111b3de2cc5b0a2855182a703c1db3
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27