NDC11 42799081601
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 |
|---|---|
| 42799-0816-01 | 42799-0816 |
| 42799-0816-1 | 42799-0816 |
| 42799-816-01 | 42799-816 |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Prednisolone Sodium Phosphate | PREDNISOLONE SODIUM PHOSPHATE | Edenbridge Pharmaceuticals LLC. | 1793e218-7b49-497d-879f-1020de6e6d68 | 2025-12-17 | Warnings, Adverse reactions | 42799-816-01 42799-816 42799081601 |