NDC11 63323010603
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 |
|---|---|
| 63323-0106-03 | 63323-0106 |
| 63323-0106-3 | 63323-0106 |
| 63323-106-03 | 63323-106 |
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 |
|---|---|---|---|---|---|---|
| magnesium sulfate | MAGNESIUM SULFATE HEPTAHYDRATE | Fresenius Kabi USA, LLC | fef9e18c-5210-4090-b564-4950ebe461c0 | 2024-04-24 | Warnings, Adverse reactions | 63323-106 |
| magnesium sulfate | MAGNESIUM SULFATE HEPTAHYDRATE | Fresenius Kabi USA, LLC | 43d658b1-2b19-44be-a346-cac11fd600b3 | 2024-04-24 | Warnings, Adverse reactions | 63323-106-03 63323-106 63323010603 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.