NDC11 00187079642
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 |
|---|---|
| 00187-0796-42 | 00187-0796 |
| 00187-796-42 | 00187-796 |
| 0187-0796-42 | 0187-0796 |
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 |
|---|---|---|---|---|---|---|
| Cardizem CD | DILTIAZEM HYDROCHLORIDE | Bausch Health US LLC | 1042fa13-e6af-46b9-8008-6c941f0978b1 | 2025-12-10 | Warnings, Adverse reactions | 0187-0796-42 0187-0796 00187079642 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.