NDC11 62037059705
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 |
|---|---|
| 62037-0597-05 | 62037-0597 |
| 62037-0597-5 | 62037-0597 |
| 62037-597-05 | 62037-597 |
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 |
|---|---|---|---|---|---|---|
| Cartia XT | DILTIAZEM HYDROCHLORIDE | Actavis Pharma, Inc. | 2dc2b889-8443-4f7f-83be-86c68e179804 | 2026-04-30 | Warnings, Adverse reactions | 62037-597-05 62037-597 62037059705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.