NDC11 64578017901
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 |
|---|---|
| 64578-0179-01 | 64578-0179 |
| 64578-0179-1 | 64578-0179 |
| 64578-179-01 | 64578-179 |
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 |
|---|---|---|---|---|---|---|
| Lymph-Tone I | ADENOSINUM CYCLOPHOSPHORICUM, APIS MELLIFICA, ARANEA DIADEMA, BELLADONNA, BOLDO, CALCAREA CARBONICA, ECHINACEA (ANGUSTIFOLIA),GALIUM APARINE, GLANDULA SUPRARENALIS SUIS, HYPOTHALAMUS (BOVINE), KALI IODATUM, PHOSPHORUS, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (VULGARIS), RHUS TOX, SCROPHULARIA NODOSA, SULPHUR, THYROIDINUM (BOVINE) | Energetix Corporation | 3fc5510e-38cb-47a5-9858-ea911c9effd7 | 2025-07-15 | Warnings | 64578-0179-1 64578-0179 64578017901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.