NDC11 82260000101
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 |
|---|---|
| 82260-0001-01 | 82260-0001 |
| 82260-0001-1 | 82260-0001 |
| 82260-001-01 | 82260-001 |
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 |
|---|---|---|---|---|---|---|
| Atropine Sulfate | ATROPINE SULFATE | Bausch & Lomb Americas Inc. | e294ce2b-6bb5-4f84-8a6d-ce2402ed926d | 2026-02-07 | Warnings, Adverse reactions | 82260-001-01 82260-001 82260000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.