NDC11 00074903730
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 |
|---|---|
| 00074-9037-30 | 00074-9037 |
| 0074-9037-30 | 0074-9037 |
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 |
|---|---|---|---|---|---|---|
| Zemplar | PARICALCITOL | AbbVie Inc. | 1b27c026-2d60-47b4-2a9c-ded1818f21b5 | 2024-08-07 | Warnings, Adverse reactions | 0074-9037-30 0074-9037 00074903730 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.