NDC11 51672531609
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 |
|---|---|
| 51672-5316-09 | 51672-5316 |
| 51672-5316-9 | 51672-5316 |
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 |
|---|---|---|---|---|---|---|
| Glycopyrrolate Oral Solution | GLYCOPYRROLATE ORAL SOLUTION | Sun Pharmaceutical Industries, Inc. | e20c9a89-2a81-3c6e-e053-2995a90a9861 | 2026-04-02 | Warnings, Adverse reactions | 51672-5316-9 51672-5316 51672531609 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.