NDC11 30142094820
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 |
|---|---|
| 30142-0948-20 | 30142-0948 |
| 30142-948-20 | 30142-948 |
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 |
|---|---|---|---|---|---|---|
| GUAIFENESIN AND DEXTROMETHORPHAN HBR | GUAIFENESIN AND DEXTROMETHORPHAN HBR | Kroger Company | 11b3c01a-93c5-4cd1-8422-d3c3d19d8dff | 2022-05-24 | Warnings | 30142-948-20 30142-948 30142094820 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.