NDC11 49702023113
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 |
|---|---|
| 49702-0231-13 | 49702-0231 |
| 49702-231-13 | 49702-231 |
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 |
|---|---|---|---|---|---|---|
| Triumeq | ABACAVIR SULFATE, DOLUTEGRAVIR SODIUM, LAMIVUDINE | ViiV Healthcare Company | 2997739a-aa91-42aa-a206-a70e2db7b84f | 2024-07-08 | Boxed warning, Warnings, Adverse reactions | 49702-231-13 49702-231 49702023113 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.