NDC11 72603020830
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 |
|---|---|
| 72603-0208-30 | 72603-0208 |
| 72603-208-30 | 72603-208 |
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 |
|---|---|---|---|---|---|---|
| arformoterol tartrate | ARFORMOTEROL TARTRATE | NorthStar RxLLC | 6a498c49-042f-481f-bc5c-a2fc00dc5668 | 2025-12-08 | Warnings, Adverse reactions | 72603-208-30 72603-208 72603020830 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.