NDC11 44911071301
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 |
|---|---|
| 44911-0713-01 | 44911-0713 |
| 44911-0713-1 | 44911-0713 |
| 44911-713-01 | 44911-713 |
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 |
|---|---|---|---|---|---|---|
| Lymphastat C | MERCURIUS SOLUBILIS, NATRUM PHOSPHORICUM, SEPIA, THUJA OCCIDENTALIS, CANDIDA PARAPSILOSIS, CANDIDA ALBICANS | Energique, Inc. | 450520fa-abbe-4546-bac2-e56c02bb81c6 | 2024-05-22 | Warnings | 44911-0713-1 44911-0713 44911071301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.