NDC11 61314024501
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 |
|---|---|
| 61314-0245-01 | 61314-0245 |
| 61314-0245-1 | 61314-0245 |
| 61314-245-01 | 61314-245 |
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 |
|---|---|---|---|---|---|---|
| Betaxolol Hydrochloride | BETAXOLOL HYDROCHLORIDE | Sandoz Inc | a73519d5-546c-4377-92ed-0d4be2685d60 | 2023-10-31 | Warnings, Adverse reactions | 61314-245-01 61314-245 61314024501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.