NDC11 50228050005
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 |
|---|---|
| 50228-0500-05 | 50228-0500 |
| 50228-0500-5 | 50228-0500 |
| 50228-500-05 | 50228-500 |
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 |
|---|---|---|---|---|---|---|
| DILTIAZEM HYDROCHLORIDE | DILTIAZEM HYDROCHLORIDE | ScieGen Pharmaceuticals, Inc. | 1ca03c9e-edc8-4c7f-89ee-f2346ea8c067 | 2025-10-16 | Warnings, Adverse reactions | 50228-500-05 50228-500 50228050005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.