NDC11 69367067901
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 |
|---|---|
| 69367-0679-01 | 69367-0679 |
| 69367-0679-1 | 69367-0679 |
| 69367-679-01 | 69367-679 |
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 |
|---|---|---|---|---|---|---|
| Hyoscyamine Sulfate ODT | HYOSCYAMINE SULFATE | Westminster Pharmaceuticals, LLC | 9429898d-301f-4ebc-8b1d-60595f76f1e3 | 2025-04-09 | Warnings, Adverse reactions | 69367-679-01 69367-679 69367067901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.