NDC 59088-0396-82
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 59088-0396-82
- Product root
- 59088-0396
- Identity scope
- Package
- Primary current NDC product row
- Not present
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.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 59088-396 | 59088-396-82 | D | Discontinued by firm | 2026-08-11 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lidocaine | LIDOCAINE | PureTek Corporation | 85e72943-6989-42f4-b519-a3ebbf4bc777 | 2025-12-12 | Warnings, Adverse reactions | 59088039682 |
| DermacinRx ZRM Pak | LIDOCAINE, DIMETHICONE | PureTek Corporation | 57c4672d-37b1-4af3-a9fc-d8390016338d | 2025-01-14 | Warnings, Adverse reactions | 59088039682 |
| DermacinRx PHN Pak | LIDOCAINE | PureTek Corporation | 8d97cb4b-ca51-49a0-b80e-701c1ca6f438 | 2024-12-06 | Warnings, Adverse reactions | 59088039682 |