NDC11 63323065120
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 |
|---|---|
| 63323-0651-20 | 63323-0651 |
| 63323-651-20 | 63323-651 |
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 |
|---|---|---|---|---|---|---|
| Adenosine | ADENOSINE | Fresenius Kabi USA, LLC | e660f71c-35ed-438e-8505-4538f5e925a2 | 2023-04-01 | Warnings, Adverse reactions | 63323-651 |
| Adenosine | ADENOSINE | Fresenius Kabi USA, LLC | f88a8cf7-d354-42f2-b5e8-ba002fcfc460 | 2023-03-02 | Warnings, Adverse reactions | 63323-651-20 63323-651 63323065120 |
| Adenosine | ADENOSINE | Fresenius Kabi USA, LLC | 6785cf30-360f-409b-a4b2-fc910728f01f | 2018-12-04 | Warnings, Adverse reactions | 63323-651 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.