NDC11 00054074287
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 |
|---|---|
| 00054-0742-87 | 00054-0742 |
| 00054-742-87 | 00054-742 |
| 0054-0742-87 | 0054-0742 |
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 |
|---|---|---|---|---|---|---|
| Albuterol Sulfate | ALBUTEROL SULFATE | Hikma Pharmaceuticals USA Inc. | 6c64ab5d-f8a2-440a-a929-cb8188d0e8b4 | 2023-01-01 | Warnings, Adverse reactions | 0054-0742-87 0054-0742 00054074287 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.