NDC11 63304045301
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 |
|---|---|
| 63304-0453-01 | 63304-0453 |
| 63304-0453-1 | 63304-0453 |
| 63304-453-01 | 63304-453 |
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 |
|---|---|---|---|---|---|---|
| Morphine sulfate | MORPHINE SULFATE | Sun Pharmaceutical Industries, Inc. | 736c9b80-682c-4cda-bf18-61b18de0bd39 | 2026-03-15 | Boxed warning, Warnings, Adverse reactions | 63304-453-01 63304-453 63304045301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.