NDC11 62135017660
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 |
|---|---|
| 62135-0176-60 | 62135-0176 |
| 62135-176-60 | 62135-176 |
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 |
|---|---|---|---|---|---|---|
| OXAPROZIN | OXAPROZIN | Chartwell RX, LLC. | db349233-9f09-471c-aeee-f91338d2ffe9 | 2024-10-23 | Boxed warning, Warnings, Adverse reactions | 62135-176-60 62135-176 62135017660 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.