NDC11 72319002502
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 |
|---|---|
| 72319-0025-02 | 72319-0025 |
| 72319-0025-2 | 72319-0025 |
| 72319-025-02 | 72319-025 |
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 |
|---|---|---|---|---|---|---|
| Maraviroc | MARAVIROC | i3 Pharmaceuticals, LLC | f7b9c67b-10c6-45b5-b2a8-952cd350b0b1 | 2023-08-18 | Boxed warning, Warnings, Adverse reactions | 72319-025-02 72319-025 72319002502 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.