NDC11 63323047141
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 |
|---|---|
| 63323-0471-41 | 63323-0471 |
| 63323-471-41 | 63323-471 |
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 |
|---|---|---|---|---|---|---|
| Haloperidol Decanoate | HALOPERIDOL DECANOATE | Fresenius Kabi USA, LLC | 262456c4-47e5-4713-8379-844f8f587495 | 2021-11-22 | Boxed warning, Warnings, Adverse reactions | 63323-471-41 63323-471 63323047141 |
| Haloperidol Decanoate | HALOPERIDOL DECANOATE | Fresenius Kabi USA, LLC | ca9896e0-fb2e-46a4-8700-20d144c14764 | 2021-09-03 | Boxed warning, Warnings, Adverse reactions | 63323-471 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.