NDC11 61755006200
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 |
|---|---|
| 61755-0062-0 | 61755-0062 |
| 61755-0062-00 | 61755-0062 |
| 61755-062-00 | 61755-062 |
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 |
|---|---|---|---|---|---|---|
| OTARMENI | LUNSOTOGENE PARVEC-CWHA | Regeneron Pharmaceuticals, Inc. | a7a5e936-ab4a-4609-ac10-96efedc89035 | 2026-04-27 | Warnings, Adverse reactions | 61755-062-00 61755-062 61755006200 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.