NDC11 37808061405
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 |
|---|---|
| 37808-0614-05 | 37808-0614 |
| 37808-0614-5 | 37808-0614 |
| 37808-614-05 | 37808-614 |
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 |
|---|---|---|---|---|---|---|
| Supreme Antacid | CALCIUM CARBONATE, MAGNESIUM HYDROXIDE | H E B | 18a7dfd9-d927-7625-e063-6394a90a270f | 2025-03-14 | Warnings | 37808-614-05 37808-614 37808061405 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.