Current NDC auxiliary source row compounder:3702

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: 72627-2434
Product Ndc: 72627-2434
Product Ndc Digits: 726272434
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Hydroxocobalamin
Proprietary Name Suffix: [empty]
Nonproprietary Name: Hydroxocobalamin
Dosage Form Name: INJECTION
Route Name: INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Empower Pharma
Establishment Name: Empower Pharma
Establishment Fei: [empty]
Substance Name: HYDROXOCOBALAMIN
Active Ingredients Info: 2 mg/1 mL
History Active Ingredients Raw: HYDROXOCOBALAMIN
History Active Ingredients Info Raw: 2 mg/1 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 72627-2434-2
Package Ndc: 72627-2434-2
Package Ndc Digits: 7262724342
Package Ndc11: 72627243402
Package Description: 10 mL in 1 VIAL, MULTI-DOSE (72627-2434-2)
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:3702
Source Row Number: 3702
Source Row Hash: 4a5d0a100a26d294fbf3fb943d90ca0e6899fba696e5fa7395e16aa950bcab2e
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27

Exact raw FDA source fields#

{
    "ROUTENAME": "INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
    "PRODUCTNDC": "72627-2434",
    "DEASCHEDULE": "",
    "LABELERNAME": "Empower Pharma",
    "SUBSTANCENAME": "HYDROXOCOBALAMIN",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "72627-2434-2",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Hydroxocobalamin",
    "REPORTINGPERIOD": "2026-1",
    "NONPROPRIETARYNAME": "Hydroxocobalamin",
    "PACKAGEDESCRIPTION": "10 mL in 1 VIAL, MULTI-DOSE (72627-2434-2) ",
    "ACTIVEINGREDIENTSINFO": "2 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:3702
Source Row Number: 3702
Status Scope: package
Lookup Ndc: 72627-2434-2
Lookup Ndc Digits: 7262724342
Product Ndc: 72627-2434
Product Ndc Digits: 726272434
Package Ndc: 72627-2434-2
Package Ndc Digits: 7262724342
Package Ndc11: 72627243402
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: 4a5d0a100a26d294fbf3fb943d90ca0e6899fba696e5fa7395e16aa950bcab2e
Import Run Id: 20261025T224840Z
Loaded At: 2026-10-25 22:53:27