NDC11 76457000400
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 |
|---|---|
| 76457-0004-0 | 76457-0004 |
| 76457-0004-00 | 76457-0004 |
| 76457-004-00 | 76457-004 |
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 |
|---|---|---|---|---|---|---|
| SIMPEX Guaifenesin | GUAIFENESIN | Simpex Pharma Pvt. Ltd | 1594f9d6-0c48-42bf-b76b-d621f215179a | 2023-11-29 | Warnings | 76457-004-00 76457-004 76457000400 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.