Current NDC auxiliary source row compounder:2132

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: 63037-164
Product Ndc: 63037-164
Product Ndc Digits: 63037164
Product Type Name: HUMAN COMPOUNDED DRUG
Proprietary Name: Lidocaine HCl
Proprietary Name Suffix: [empty]
Nonproprietary Name: Lidocaine HCl 2%
Dosage Form Name: INJECTION
Route Name: INFILTRATION
Marketing Category Name: OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
Labeler Name: Hikma Injectables USA Inc.
Establishment Name: Hikma Injectables USA Inc.
Establishment Fei: [empty]
Substance Name: LIDOCAINE HYDROCHLORIDE ANHYDROUS
Active Ingredients Info: 100 mg/5 mL
History Active Ingredients Raw: LIDOCAINE HYDROCHLORIDE ANHYDROUS
History Active Ingredients Info Raw: 100 mg/5 mL
History Dosage Raw: INJECTION
Dea Schedule: [empty]
Package Ndc Raw: 63037-164-25
Package Ndc: 63037-164-25
Package Ndc Digits: 6303716425
Package Ndc11: 63037016425
Package Description: 5 mL in 1 SYRINGE, PLASTIC (63037-164-25)
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
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:2132
Source Row Number: 2132
Source Row Hash: 4a565fb37c0f98af22f66d3972edbe5e1adea6f554c62c1f08fd5d347fed3de3
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01

Exact raw FDA source fields#

{
    "ROUTENAME": "INFILTRATION",
    "PRODUCTNDC": "63037-164",
    "DEASCHEDULE": "",
    "LABELERNAME": "Hikma Injectables USA Inc.",
    "SUBSTANCENAME": "LIDOCAINE HYDROCHLORIDE ANHYDROUS",
    "DOSAGEFORMNAME": "INJECTION",
    "NDCPACKAGECODE": "63037-164-25",
    "PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
    "PROPRIETARYNAME": "Lidocaine HCl",
    "REPORTINGPERIOD": "2024-2",
    "NONPROPRIETARYNAME": "Lidocaine HCl 2%",
    "PACKAGEDESCRIPTION": "5 mL in 1 SYRINGE, PLASTIC (63037-164-25) ",
    "ACTIVEINGREDIENTSINFO": "100 mg/5 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:2132
Source Row Number: 2132
Status Scope: package
Lookup Ndc: 63037-164-25
Lookup Ndc Digits: 6303716425
Product Ndc: 63037-164
Product Ndc Digits: 63037164
Package Ndc: 63037-164-25
Package Ndc Digits: 6303716425
Package Ndc11: 63037016425
Product Id: [empty]
Status Code: COMPOUNDER
Status Label: Outsourcing facility compounded drug report
Reporting Period Raw: 2024-2
Reporting Period: 2024-2
Source Table: fda_ndc_aux_compounder
Source File: compounders_ndc_directory.txt
Source Date: 2026-09-18
Source Row Hash: 4a565fb37c0f98af22f66d3972edbe5e1adea6f554c62c1f08fd5d347fed3de3
Import Run Id: 20261024T140201Z
Loaded At: 2026-10-24 14:07:01