NDC11 84989002501
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 |
|---|---|
| 84989-0025-01 | 84989-0025 |
| 84989-0025-1 | 84989-0025 |
| 84989-025-01 | 84989-025 |
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 |
|---|---|---|---|---|---|---|
| PUTRIZEN 40 UREA | GLYCERIN | Shantou Ximonth Biotechnology Co., Ltd. | 533dadbc-6f20-d880-e063-6394a90a753f | 2026-06-01 | Warnings | 84989-025-01 84989-025 84989002501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.