NDC11 44911064701
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 |
|---|---|
| 44911-0647-01 | 44911-0647 |
| 44911-0647-1 | 44911-0647 |
| 44911-647-01 | 44911-647 |
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 |
|---|---|---|---|---|---|---|
| Lymphdrainex | GERANIUM ROBERTIANUM, NASTURTIUM AQUATICUM, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA, APIS MELLIFICA, EQUISETUM HYEMALE, FUMARIA OFFICINALIS, NATRUM SULPHURICUM, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, VERONICA OFFICINALIS, ALOE, GENTIANA LUTEA, JUGLANS REGIA, MYOSOTIS ARVENSIS, SARSAPARILLA (SMILAX REGELII), BARYTA CARBONICA, HEPAR SULPHURIS CALCAREUM, MERCURIUS CYANATUS, FERRUM IODATUM, ARANEA DIADEMA, CALCAREA PHOSPHORICA, PARATHYROID GLAND (BOVINE), THYMUS (SUIS), THYROIDINUM (SUIS) | Energique, Inc. | daa2aa55-0db4-4ebe-bdda-b1611258a78f | 2023-12-04 | Warnings | 44911-0647-1 44911-0647 44911064701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.