Current NDC auxiliary source row compounder:2541

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: 69194-210
Product Ndc: 69194-210
Product Ndc Digits: 69194210
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: 210 CALCIUM CHLORIDE 20MG/ML BAG
Proprietary Name Suffix: [empty]
Nonproprietary Name: calcium chloride
Dosage Form Name: INJECTION
Route Name: INTRAVENOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Pine Pharmaceuticals LLC
Establishment Name: Pine Pharmaceuticals LLC
Establishment Fei: [empty]
Substance Name: CALCIUM CHLORIDE
Active Ingredients Info: 20 mg/1 mL
History Active Ingredients Raw: CALCIUM CHLORIDE
History Active Ingredients Info Raw: 20 mg/1 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 69194-210-01
Package Ndc: 69194-210-01
Package Ndc Digits: 6919421001
Package Ndc11: 69194021001
Package Description: 500 mL in 1 BAG (69194-210-01)
Reporting Period Raw: 2026-1
Reporting Period: 2026-1
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:2541
Source Row Number: 2541
Source Row Hash: 85359907c0a82a05784eb275c0d3fba93c385a8b686cc87045beac0b8b24acb3
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAVENOUS",
    "PRODUCTNDC": "69194-210",
    "DEASCHEDULE": "",
    "LABELERNAME": "Pine Pharmaceuticals LLC",
    "SUBSTANCENAME": "CALCIUM CHLORIDE",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "69194-210-01",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "210 CALCIUM CHLORIDE 20MG/ML BAG",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "calcium chloride",
    "PACKAGEDESCRIPTION": "500 mL in 1 BAG (69194-210-01) ",
    "ACTIVEINGREDIENTSINFO": "20 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:2541
Source Row Number: 2541
Status Scope: package
Lookup Ndc: 69194-210-01
Lookup Ndc Digits: 6919421001
Product Ndc: 69194-210
Product Ndc Digits: 69194210
Package Ndc: 69194-210-01
Package Ndc Digits: 6919421001
Package Ndc11: 69194021001
Product Id: [empty]
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: 85359907c0a82a05784eb275c0d3fba93c385a8b686cc87045beac0b8b24acb3
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01