NDC11 63323006441
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 |
|---|---|
| 63323-0064-41 | 63323-0064 |
| 63323-064-41 | 63323-064 |
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 | e921a46b-9a5b-4163-9c88-224247541f14 | 2026-01-13 | Warnings, Adverse reactions | 63323-064 |
| Magnesium Sulfate | MAGNESIUM SULFATE HEPTAHYDRATE | Fresenius Kabi USA, LLC | e9c10579-29f3-4889-8881-0626f63968d4 | 2026-01-12 | Warnings, Adverse reactions | 63323-064 |
| Magnesium Sulfate | MAGNESIUM SULFATE HEPTAHYDRATE | Fresenius Kabi USA, LLC | 6a5d362b-7aa7-40d3-898d-09407cce0713 | 2026-01-08 | Warnings, Adverse reactions | 63323-064-41 63323-064 63323006441 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.