NDC11 66096074908
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 |
|---|---|
| 66096-0749-08 | 66096-0749 |
| 66096-0749-8 | 66096-0749 |
| 66096-749-08 | 66096-749 |
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 |
|---|---|---|---|---|---|---|
| Spongilla lacustris MT | SPONGILLA LACUSTRIS | OHM PHARMA INC. | a855d4ca-52ed-4e69-93b5-7304bcc84f73 | 2021-12-29 | Warnings | 66096-749-08 66096-749 66096074908 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.