NDC11 71921011101
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 |
|---|---|
| 71921-0111-01 | 71921-0111 |
| 71921-0111-1 | 71921-0111 |
| 71921-111-01 | 71921-111 |
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 | GLYCOPYRROLATE | Florida Pharmaceutical Products, LLC | 2cda1ed5-10bb-4651-acbf-be44ad709665 | 2026-02-12 | Warnings, Adverse reactions | 71921-111-01 71921-111 71921011101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.