NDC11 43857015901
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 |
|---|---|
| 43857-0159-01 | 43857-0159 |
| 43857-0159-1 | 43857-0159 |
| 43857-159-01 | 43857-159 |
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 |
|---|---|---|---|---|---|---|
| Arterioforce I | ARNICA MONTANA, LILIUM TIGRINUM, AURUM MURIATICUM, CACTUS GRANDIFLORUS, DIGITALIS PURPUREA, GLONOINUM, NUX VOMICA, VERATRUM ALBUM | BioActive Nutritional, Inc. | 4f068076-413d-49e9-997c-57cfc22eb080 | 2025-05-16 | Warnings | 43857-0159-1 43857-0159 43857015901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.