FDA.reportPublic FDA data

NDC11 59088039682

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
59088-0396-8259088-0396
59088-396-8259088-396

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 packagepackage59088-39659088-396-82DDiscontinued by firm2026-08-11

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): 59088-396-82
ndc (product): 59088-396
ndc11 (package): 59088039682
DermacinRx ZRM PakLIDOCAINE, DIMETHICONEPureTek Corporation57c4672d-37b1-4af3-a9fc-d8390016338d2025-01-14Warnings, Adverse reactionsExact identifier
ndc (package): 59088-396-82
ndc11 (package): 59088039682
DermacinRx PHN PakLIDOCAINEPureTek Corporation8d97cb4b-ca51-49a0-b80e-701c1ca6f4382024-12-06Warnings, Adverse reactionsExact identifier
ndc (package): 59088-396-82
ndc11 (package): 59088039682