Current NDC auxiliary source row compounder:111
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
- 70092-658
- Product Ndc
- 70092-658
- Product Ndc Digits
- 70092658
- Product Type Name
- HUMAN COMPOUNDED DRUG
- Proprietary Name
- L.E.T. Solution 3 ml in 5 ml TS
- Proprietary Name Suffix
- Nonproprietary Name
- L.E.T. Solution 3 ml in 5 ml TS
- Dosage Form Name
- SOLUTION
- Route Name
- TOPICAL
- Marketing Category Name
- OUTSOURCING FACILITY COMPOUNDED HUMAN DRUG PRODUCT (EXEMPT FROM APPROVAL REQUIREMENTS)
- Labeler Name
- QuVa Pharma, Inc.
- Establishment Name
- QuVa Pharma, Inc.
- Establishment Fei
- Substance Name
- LIDOCAINE HYDROCHLORIDE ANHYDROUS; TETRACAINE HYDROCHLORIDE; EPINEPHRINE HYDROCHLORIDE
- Active Ingredients Info
- 120 mg/3 mL; 15 mg/3 mL; 1.5 mg/3 mL
- History Active Ingredients Raw
- LIDOCAINE HYDROCHLORIDE ANHYDROUS; TETRACAINE HYDROCHLORIDE; EPINEPHRINE HYDROCHLORIDE
- History Active Ingredients Info Raw
- 120 mg/3 mL; 15 mg/3 mL; 1.5 mg/3 mL
- History Dosage Raw
- SOLUTION
- Dea Schedule
- Package Ndc Raw
- 70092-658-44
- Package Ndc
- 70092-658-44
- Package Ndc Digits
- 7009265844
- Package Ndc11
- 70092065844
- Package Description
- 3 mL in 1 SYRINGE (70092-658-44)
- Reporting Period Raw
- 2024-2
- Reporting Period
- 2024-2
- Normalization Status
- valid
- 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:111
- Source Row Number
- 111
- Source Row Hash
- 395c62e19fb5d790dba38bf960667873a4865b38216509915da282597ef62526
- Import Run Id
- 20261018T022251Z
- Loaded At
- 2026-10-18 02:29:51
Exact raw FDA source fields#
{
"ROUTENAME": "TOPICAL",
"PRODUCTNDC": "70092-658",
"DEASCHEDULE": "",
"LABELERNAME": "QuVa Pharma, Inc.",
"SUBSTANCENAME": "LIDOCAINE HYDROCHLORIDE ANHYDROUS; TETRACAINE HYDROCHLORIDE; EPINEPHRINE HYDROCHLORIDE",
"DOSAGEFORMNAME": "SOLUTION",
"NDCPACKAGECODE": "70092-658-44",
"PRODUCTTYPENAME": "HUMAN COMPOUNDED DRUG",
"PROPRIETARYNAME": "L.E.T. Solution 3 ml in 5 ml TS",
"REPORTINGPERIOD": "2024-2",
"NONPROPRIETARYNAME": "L.E.T. Solution 3 ml in 5 ml TS",
"PACKAGEDESCRIPTION": "3 mL in 1 SYRINGE (70092-658-44) ",
"ACTIVEINGREDIENTSINFO": "120 mg/3 mL; 15 mg/3 mL; 1.5 mg/3 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:111
- Source Row Number
- 111
- Status Scope
- package
- Lookup Ndc
- 70092-658-44
- Lookup Ndc Digits
- 7009265844
- Product Ndc
- 70092-658
- Product Ndc Digits
- 70092658
- Package Ndc
- 70092-658-44
- Package Ndc Digits
- 7009265844
- Package Ndc11
- 70092065844
- Product Id
- 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
- 395c62e19fb5d790dba38bf960667873a4865b38216509915da282597ef62526
- Import Run Id
- 20261018T022251Z
- Loaded At
- 2026-10-18 02:29:51