NDC11 66096078801
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 |
|---|---|
| 66096-0788-01 | 66096-0788 |
| 66096-0788-1 | 66096-0788 |
| 66096-788-01 | 66096-788 |
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 |
|---|---|---|---|---|---|---|
| Argentum Muriaticum | ARGENTUM MURIATICUM | OHM PHARMA INC. | ee1b7610-8d6e-4c65-86a0-b38b8a051c4c | 2021-01-14 | Warnings | 66096-788-01 66096-788 66096078801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.