NDC11 37662304001
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 |
|---|---|
| 37662-3040-01 | 37662-3040 |
| 37662-3040-1 | 37662-3040 |
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 |
|---|---|---|---|---|---|---|
| Rubidium Fluoratum | RUBIDIUM FLUORATUM | Hahnemann Laboratories, INC. | fa47c370-d4b2-9d82-e053-6294a90a8551 | 2023-04-26 | 37662-3040-1 37662-3040 37662304001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.