NDC11 69676009804
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 |
|---|---|
| 69676-0098-04 | 69676-0098 |
| 69676-0098-4 | 69676-0098 |
| 69676-098-04 | 69676-098 |
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 |
|---|---|---|---|---|---|---|
| Genexa Antacid Maximum Strength | CALCIUM CARBONATE | Genexa Inc. | 3a39d91c-2dcd-71d6-e063-6394a90a5474 | 2026-08-22 | Warnings | 69676-0098-4 69676-0098 69676009804 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.