NDC11 67877050030
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 |
|---|---|
| 67877-0500-30 | 67877-0500 |
| 67877-500-30 | 67877-500 |
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 |
|---|---|---|---|---|---|---|
| Amlodipine and olmesartan Medoxomil | AMLODIPINE AND OLMESARTAN MEDOXOMIL | Ascend Laboratories, LLC | c1204fbe-d086-43cf-bbaa-efec9cd0487c | 2025-05-30 | Boxed warning, Warnings, Adverse reactions | 67877-500-30 67877-500 67877050030 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.