NDC11 73043005196
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 |
|---|---|
| 73043-0051-96 | 73043-0051 |
| 73043-051-96 | 73043-051 |
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 |
|---|---|---|---|---|---|---|
| Formoterol fumarate | FORMOTEROL FUMARATE DIHYDRATE | Devatis, Inc. | fd0dac5d-e58c-46ee-9d28-1a1ef7a6be5e | 2025-04-10 | Warnings, Adverse reactions | 73043-051-96 73043-051 73043005196 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.