NDC11 63323040703
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 |
|---|---|
| 63323-0407-03 | 63323-0407 |
| 63323-0407-3 | 63323-0407 |
| 63323-407-03 | 63323-407 |
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 |
|---|---|---|---|---|---|---|
| Caffeine Citrate | CAFFEINE CITRATE | Fresenius Kabi USA, LLC | baf9f88a-776a-44e7-82cc-8f0ca419572f | 2023-07-20 | Warnings, Adverse reactions | 63323-407-03 63323-407 63323040703 |
| Caffeine Citrate | CAFFEINE CITRATE | Fresenius Kabi USA, LLC | 38b39044-737a-4247-a6c4-c86f5e92490e | 2023-07-14 | Warnings, Adverse reactions | 63323-407 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.