NDC11 63323066441
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 |
|---|---|
| 63323-0664-41 | 63323-0664 |
| 63323-664-41 | 63323-664 |
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 |
|---|---|---|---|---|---|---|
| Diphenhydramine | DIPHENHYDRAMINE HYDROCHLORIDE | Fresenius Kabi USA, LLC | fc574e74-1fdc-4a61-a1ed-492ae43faed2 | 2025-02-21 | Warnings, Adverse reactions | 63323-664 |
| Diphenhydramine | DIPHENHYDRAMINE HYDROCHLORIDE | Fresenius Kabi USA, LLC | 921b9f64-1096-46db-866a-67f0f9ff6790 | 2024-10-14 | Warnings, Adverse reactions | 63323-664-41 63323-664 63323066441 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.