NDC11 00019133265
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 |
|---|---|
| 00019-1332-65 | 00019-1332 |
| 0019-1332-65 | 0019-1332 |
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 | 0019-1332 | 0019-1332-65 | D | Discontinued by firm | 2026-10-05 |
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 |
|---|---|---|---|---|---|---|
| Optiray 320 | IOVERSOL | Liebel-Flarsheim Company LLC | 6cb6ca5f-b249-49b0-a9eb-8aa583da7c74 | 2025-12-29 | Boxed warning, Warnings, Adverse reactions | 0019-1332 |
| Optiray 320 | IOVERSOL | Liebel-Flarsheim Company LLC | cd718d1c-f813-4114-a50d-c744ff7eb1bf | 2025-12-29 | Boxed warning, Warnings, Adverse reactions | 0019-1332-65 0019-1332 00019133265 |
| Optiray 320 | IOVERSOL | Liebel-Flarsheim Company LLC | 549d38db-d4ed-4708-8f76-7cdaa157063f | 2023-02-17 | Boxed warning, Warnings, Adverse reactions | 0019-1332 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.