NDC11 46708056530
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 |
|---|---|
| 46708-0565-30 | 46708-0565 |
| 46708-565-30 | 46708-565 |
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 |
|---|---|---|---|---|---|---|
| ERLOTINIB HYDROCHLORIDE | ERLOTINIB HYDROCHLORIDE | Alembic Pharmaceuticals Limited | ab6f3cb3-34a8-4492-a5d7-fb6b055a2d6b | 2024-06-10 | Warnings, Adverse reactions | 46708-565-30 46708-565 46708056530 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.