NDC11 31722053501
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 |
|---|---|
| 31722-0535-01 | 31722-0535 |
| 31722-0535-1 | 31722-0535 |
| 31722-535-01 | 31722-535 |
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 |
|---|---|---|---|---|---|---|
| Tenofovir Disoproxil Fumarate | TENOFOVIR DISOPROXIL FUMARATE | Camber Pharmaceuticals, Inc. | 1ac4c628-f01f-42d4-b8e6-d12273aefc6d | 2023-01-26 | Boxed warning, Warnings, Adverse reactions | 31722-535-01 31722-535 31722053501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.