FDA.reportPublic FDA data

NDC11 59088039654

This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.

Possible FDA NDC forms#

Package NDC, Product root table
Package NDCProduct root
59088-0396-5459088-0396
59088-396-5459088-396

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59088-39659088-396-54DDiscontinued by firm2026-08-17

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 3 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
LidocaineLIDOCAINEPureTek Corporation85e72943-6989-42f4-b519-a3ebbf4bc7772025-12-12Warnings, Adverse reactionsExact identifier
ndc (package): 59088-396-54
ndc (product): 59088-396
ndc11 (package): 59088039654
LidoxrylLIDOCAINEPureTek Corporation1c33790b-8d57-46e8-bd6e-5a0f87a3c29f2020-11-10Warnings, Adverse reactionsExact identifier
ndc (package): 59088-396-54
ndc11 (package): 59088039654
LidoPure PatchLIDOCAINEPureTek Corporationc851c6e9-1966-4639-9406-fe6adc91c9d02020-11-10Warnings, Adverse reactionsExact identifier
ndc (package): 59088-396-54
ndc11 (package): 59088039654