NDC11 68180035502
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 |
|---|---|
| 68180-0355-02 | 68180-0355 |
| 68180-0355-2 | 68180-0355 |
| 68180-355-02 | 68180-355 |
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 |
|---|---|---|---|---|---|---|
| RANOLAZINE | RANOLAZINE | Lupin Pharmaceuticals, Inc. | 595821d7-1fbf-49a5-9c62-d78f27af39b4 | 2023-12-08 | Warnings, Adverse reactions | 68180-355-02 68180-355 68180035502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.