NDC11 76457000100
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 |
|---|---|
| 76457-0001-0 | 76457-0001 |
| 76457-0001-00 | 76457-0001 |
| 76457-001-00 | 76457-001 |
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 |
|---|---|---|---|---|---|---|
| Aluminum hydroxide and Magnesium carbonate | ALUMINUM HYDROXIDE, MAGNESIUM CARBONATE | Simpex Pharma Pvt. Ltd | e799a555-bfd0-4298-a5dc-aeb671815d40 | 2023-11-29 | Warnings | 76457-001-00 76457-001 76457000100 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.