NDC11 60986204003
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 |
|---|---|
| 60986-2040-03 | 60986-2040 |
| 60986-2040-3 | 60986-2040 |
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 |
|---|---|---|---|---|---|---|
| AB | ACONITUM NAPELLUS, BRYONIA CRETICA | MARCO PHARMA INTERNATIONAL LLC | 2d81c13f-102a-6741-e063-6294a90aee84 | 2026-01-12 | Warnings | 60986-2040-3 60986-2040 60986204003 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.