NDC11 72603072101
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 |
|---|---|
| 72603-0721-01 | 72603-0721 |
| 72603-0721-1 | 72603-0721 |
| 72603-721-01 | 72603-721 |
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 |
|---|---|---|---|---|---|---|
| Candesartan | CANDESARTAN | NorthStar RxLLC | 880f685f-be01-42f4-9e76-ebd1fcfb1f77 | 2025-11-26 | Boxed warning, Warnings, Adverse reactions | 72603-721-01 72603-721 72603072101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.