NDC11 70377004913
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 |
|---|---|
| 70377-0049-13 | 70377-0049 |
| 70377-049-13 | 70377-049 |
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 |
|---|---|---|---|---|---|---|
| Lenalidomide | LENALIDOMIDE | BIOCON PHARMA INC., | ed7a3099-ce31-4865-b212-358d9ff6261b | 2025-03-03 | Boxed warning, Warnings, Adverse reactions | 70377-049-13 70377-049 70377004913 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.