NDC11 49702023803
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 |
|---|---|
| 49702-0238-03 | 49702-0238 |
| 49702-0238-3 | 49702-0238 |
| 49702-238-03 | 49702-238 |
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 |
|---|---|---|---|---|---|---|
| Apretude | CABOTEGRAVIR | ViiV Healthcare Company | 4338428e-43d4-4e02-ac9d-bd98e738a7da | 2025-04-11 | Boxed warning, Warnings, Adverse reactions | 49702-238-03 49702023803 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.