NDC11 82509000160
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 |
|---|---|
| 82509-0001-60 | 82509-0001 |
| 82509-001-60 | 82509-001 |
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 |
|---|---|---|---|---|---|---|
| encer | CADMIUM SULPHURATUM, CARBO ANIMALIS, PHOSPHORICUM ACIDUM, RADIUM BROMATUM, X-RAY | B'OKCARES LTD | 5d7bce73-077c-41c5-9b6b-8580dc79dc40 | 2025-12-29 | Warnings | 82509-001-60 82509-001 82509000160 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.