NDC11 00517610125
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 |
|---|---|
| 00517-6101-25 | 00517-6101 |
| 0517-6101-25 | 0517-6101 |
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 |
|---|---|---|---|---|---|---|
| Zinc Sulfate | ZINC SULFATE | American Regent, Inc. | 4b528c88-07a0-4dce-84c6-ccd32555bbff | 2020-10-01 | Warnings, Adverse reactions | 0517-6101-25 0517-6101 00517610125 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.