NDC11 16714053401
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 |
|---|---|
| 16714-0534-01 | 16714-0534 |
| 16714-0534-1 | 16714-0534 |
| 16714-534-01 | 16714-534 |
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 |
|---|---|---|---|---|---|---|
| Emtricitabine and tenofovir disoproxil fumarate | EMTRICITABINE AND TENOFOVIR DISOPROXIL FUMARATE | NorthStar RxLLC | fbbc7b73-eddf-40b5-8ebb-7b3d9c42dba6 | 2022-07-25 | Boxed warning, Warnings, Adverse reactions | 16714-534-01 16714-534 16714053401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.