NDC11 51662161101
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 |
|---|---|
| 51662-1611-01 | 51662-1611 |
| 51662-1611-1 | 51662-1611 |
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 |
|---|---|---|---|---|---|---|
| GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE) | GRAFCO SILVER NITRATE (75% SILVER NITRATE, 25% POTASSIUM NITRATE) | HF Acquisition Co LLC, DBA HealthFirst | e5ebf7aa-fbe5-45b1-e053-2a95a90a5cbf | 2024-03-25 | Warnings | 51662-1611-1 51662-1611 51662161101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.