NDC11 44911059301
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 |
|---|---|
| 44911-0593-01 | 44911-0593 |
| 44911-0593-1 | 44911-0593 |
| 44911-593-01 | 44911-593 |
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 |
|---|---|---|---|---|---|---|
| COUGHTONE | ECHINACEA, LOBELIA INFLATA, ANTIMONIUM TARTARICUM, ARALIA RACEMOSA, DROSERA (ROTUNDIFOLIA), IPECACUANHA, KALI CARBONICUM, PHOSPHORUS, SPONGIA TOSTA | Energique, Inc. | 0d4514ca-fbe0-4139-8151-aad039ccf05a | 2024-01-23 | Warnings | 44911-0593-1 44911-0593 44911059301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.