Current NDC auxiliary source row compounder:635

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: 71266-1025
Product Ndc: 71266-1025
Product Ndc Digits: 712661025
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Betamethasone Sodium Phosphate
Proprietary Name Suffix: [empty]
Nonproprietary Name: Betamethasone Sodium Phosphate
Dosage Form Name: INJECTION
Route Name: EPIDURAL; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Fagron Compounding Services LLC dba Fagron Sterile Services LLC dba JCB Laboratories
Establishment Name: Fagron Compounding Services LLC dba Fagron Sterile Services LLC dba JCB Laboratories
Establishment Fei: [empty]
Substance Name: BETAMETHASONE SODIUM PHOSPHATE
Active Ingredients Info: 6 mg/1 mL
History Active Ingredients Raw: BETAMETHASONE SODIUM PHOSPHATE
History Active Ingredients Info Raw: 6 mg/1 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 71266-1025-2
Package Ndc: 71266-1025-2
Package Ndc Digits: 7126610252
Package Ndc11: 71266102502
Package Description: 2 mL in 1 VIAL (71266-1025-2)
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:635
Source Row Number: 635
Source Row Hash: 03c12ea7aaa431d9ab2107de3b4ab9ed29f2bcdea284cbe1e65c08dc1d9f789a
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51

Exact raw FDA source fields#

{
    "ROUTENAME": "EPIDURAL; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR",
    "PRODUCTNDC": "71266-1025",
    "DEASCHEDULE": "",
    "LABELERNAME": "Fagron Compounding Services LLC dba Fagron Sterile Services LLC dba JCB Laboratories",
    "SUBSTANCENAME": "BETAMETHASONE SODIUM PHOSPHATE",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "71266-1025-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Betamethasone Sodium Phosphate",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Betamethasone Sodium Phosphate",
    "PACKAGEDESCRIPTION": "2 mL in 1 VIAL (71266-1025-2) ",
    "ACTIVEINGREDIENTSINFO": "6 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:635
Source Row Number: 635
Status Scope: package
Lookup Ndc: 71266-1025-2
Lookup Ndc Digits: 7126610252
Product Ndc: 71266-1025
Product Ndc Digits: 712661025
Package Ndc: 71266-1025-2
Package Ndc Digits: 7126610252
Package Ndc11: 71266102502
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: 03c12ea7aaa431d9ab2107de3b4ab9ed29f2bcdea284cbe1e65c08dc1d9f789a
Import Run Id: 20261018T022251Z
Loaded At: 2026-10-18 02:29:51