NDC11 42708008221
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 |
|---|---|
| 42708-0082-21 | 42708-0082 |
| 42708-082-21 | 42708-082 |
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 |
|---|---|---|---|---|---|---|
| BENZONATATE | BENZONATATE | QPharma, Inc. | 55c4ae18-3e37-4caf-9fdb-9d307970b5f9 | 2025-12-21 | Warnings, Adverse reactions | 42708-082-21 42708-082 42708008221 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.