NDC11 00143919901
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 |
|---|---|
| 00143-9199-01 | 00143-9199 |
| 00143-9199-1 | 00143-9199 |
| 0143-9199-01 | 0143-9199 |
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 |
|---|---|---|---|---|---|---|
| Olanzapine | OLANZAPINE | Hikma Pharmaceuticals USA Inc. | 63bcfe98-d1fc-4cd7-9212-f59ee4dcc6d1 | 2026-08-25 | Boxed warning, Warnings, Adverse reactions | 0143-9199-01 0143-9199 00143919901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.