NDC11 63323022930
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 |
|---|---|
| 63323-0229-30 | 63323-0229 |
| 63323-229-30 | 63323-229 |
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 |
|---|---|---|---|---|---|---|
| Protamine Sulfate | PROTAMINE SULFATE | Fresenius Kabi USA, LLC | e1964129-33f4-4e4e-86e3-8e6a4e65bd83 | 2025-02-05 | Boxed warning, Warnings, Adverse reactions | 63323-229-30 63323-229 63323022930 |
| Protamine Sulfate | PROTAMINE SULFATE | Fresenius Kabi USA, LLC | 7a31fc4c-579f-45cc-9559-39cfad9a57b3 | 2024-03-18 | Boxed warning, Warnings, Adverse reactions | 63323-229 |
| Protamine Sulfate | PROTAMINE SULFATE | Fresenius Kabi USA, LLC | 8df0a819-9e1a-44ce-97a6-3ea82c867d44 | 2024-01-18 | Boxed warning, Warnings, Adverse reactions | 63323-229 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.