NDC11 72673007301
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 |
|---|---|
| 72673-0073-01 | 72673-0073 |
| 72673-0073-1 | 72673-0073 |
| 72673-073-01 | 72673-073 |
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 |
|---|---|---|---|---|---|---|
| Amiodarone Hydrochloride | AMIODARONE HYDROCHLORIDE | Zhejiang Poly Pharm. Co., Ltd. | 0a28ae25-7cc4-4ac0-a2ba-7820fb93e25c | 2026-01-16 | Warnings, Adverse reactions | 72673-073-01 72673-073 72673007301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.