NDC11 00009009401
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 |
|---|---|
| 00009-0094-01 | 00009-0094 |
| 00009-0094-1 | 00009-0094 |
| 00009-094-01 | 00009-094 |
| 0009-0094-01 | 0009-0094 |
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 |
|---|---|---|---|---|---|---|
| Xanax | ALPRAZOLAM | PHARMACIA & UPJOHN COMPANY LLC | 388e249d-b9b6-44c3-9f8f-880eced0239f | 2023-01-18 | Boxed warning, Warnings, Adverse reactions | 0009-0094-01 0009-0094 00009009401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.