NDC11 66077069301
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 |
|---|---|
| 66077-0693-01 | 66077-0693 |
| 66077-0693-1 | 66077-0693 |
| 66077-693-01 | 66077-693 |
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 |
|---|---|---|---|---|---|---|
| INSTANT | INSTANT | Ultra-Chem, Inc. | 0c425c6e-6c05-1748-e063-6394a90a9b5e | 2023-12-11 | Warnings | 66077-693-01 66077-693 66077069301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.