NDC11 63304019290
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 |
|---|---|
| 63304-0192-90 | 63304-0192 |
| 63304-192-90 | 63304-192 |
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 |
|---|---|---|---|---|---|---|
| Desvenlafaxine | DESVENLAFAXINE | Sun Pharmaceutical Industries, Inc. | 91cf39c9-4d26-480a-a3a3-a3d8d4c4d222 | 2023-08-07 | Boxed warning, Warnings, Adverse reactions | 63304-192-90 63304-192 63304019290 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.