NDC11 72266010301
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 |
|---|---|
| 72266-0103-01 | 72266-0103 |
| 72266-0103-1 | 72266-0103 |
| 72266-103-01 | 72266-103 |
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 |
|---|---|---|---|---|---|---|
| Labetalol Hydrochloride | LABETALOL HYDROCHLORIDE | Fosun Pharma USA Inc. | 4a5ffab2-a3b8-411e-992d-7f38d508643a | 2024-05-16 | Warnings, Adverse reactions | 72266-103-01 72266-103 72266010301 |
| Labetalol Hydrochloride | LABETALOL HYDROCHLORIDE | Fosun Pharma USA Inc. | f18dff28-f6f5-4ecb-9797-25062e247559 | 2021-01-28 | Warnings, Adverse reactions | 72266-103 |