NDC11 64578017001
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 |
|---|---|
| 64578-0170-01 | 64578-0170 |
| 64578-0170-1 | 64578-0170 |
| 64578-170-01 | 64578-170 |
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 |
|---|---|---|---|---|---|---|
| Endopath-F | AGNUS, ANGELICA SIN, CIMICIFUGA, FUCUS, GLANDULA SUPRARENALIS SUIS, GLYCYRRHIZA, HYPOTHALAMUS, OOPHORINUM, PITUITARUM POSTERIUM, PULSATILLA, SEPIA, THYROIDINUM, XANTHOXYLUM | Energetix Corporation | d0880c30-54f5-4af4-ad5d-85ecae3bb9e5 | 2025-07-15 | Warnings | 64578-0170-1 64578-0170 64578017001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.