NDC11 24338001009
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 |
|---|---|
| 24338-0010-09 | 24338-0010 |
| 24338-0010-9 | 24338-0010 |
| 24338-010-09 | 24338-010 |
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 |
|---|---|---|---|---|---|---|
| BiDil | HYDRALAZINE HYDROCHLORIDE AND ISOSORBIDE DINITRATE | Azurity Pharmaceuticals, Inc. | e1e63cd5-d1e4-4af5-bad5-1ad41ea46b00 | 2025-11-30 | Warnings, Adverse reactions | 24338-010-09 24338-010 24338001009 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.