Current NDC auxiliary source row compounder:94

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: 71300-6635
Product Ndc: 71300-6635
Product Ndc Digits: 713006635
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Baclofen
Proprietary Name Suffix: [empty]
Nonproprietary Name: Baclofen
Dosage Form Name: CREAM
Route Name: TOPICAL
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Nubratori Inc.
Establishment Name: Nubratori Inc.
Establishment Fei: [empty]
Substance Name: BACLOFEN
Active Ingredients Info: 20 mg/1 g
History Active Ingredients Raw: BACLOFEN
History Active Ingredients Info Raw: 20 mg/1 g
History Dosage Raw: CREAM
Dea Schedule: [empty]
Package Ndc Raw: 71300-6635-4
Package Ndc: 71300-6635-4
Package Ndc Digits: 7130066354
Package Ndc11: 71300663504
Package Description: 1 CONTAINER in 1 BOX (71300-6635-4) > 30 g in 1 CONTAINER
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:94
Source Row Number: 94
Source Row Hash: d981044b65f4f35619e7b44541d5999fc115d9133d350d99dded3acc443fa967
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20

Exact raw FDA source fields#

{
    "ROUTENAME": "TOPICAL",
    "PRODUCTNDC": "71300-6635",
    "DEASCHEDULE": "",
    "LABELERNAME": "Nubratori Inc.",
    "SUBSTANCENAME": "BACLOFEN",
    "DOSAGEFORMNAME": "CREAM",
    "NDCPACKAGECODE": "71300-6635-4",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Baclofen",
    "REPORTINGPERIOD": "2025-1",
    "NONPROPRIETARYNAME": "Baclofen",
    "PACKAGEDESCRIPTION": "1 CONTAINER in 1 BOX (71300-6635-4)  > 30 g in 1 CONTAINER",
    "ACTIVEINGREDIENTSINFO": "20 mg/1 g",
    "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:94
Source Row Number: 94
Status Scope: package
Lookup Ndc: 71300-6635-4
Lookup Ndc Digits: 7130066354
Product Ndc: 71300-6635
Product Ndc Digits: 713006635
Package Ndc: 71300-6635-4
Package Ndc Digits: 7130066354
Package Ndc11: 71300663504
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: d981044b65f4f35619e7b44541d5999fc115d9133d350d99dded3acc443fa967
Import Run Id: 20261015T162751Z
Loaded At: 2026-10-15 16:32:20