NDC11 64578009901

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 table
Package NDC	Product root
64578-0099-01	64578-0099
64578-0099-1	64578-0099
64578-099-01	64578-099

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Endopath-M	ADENOSINUM CYCLOPHOSPHORICUM, AGNUS CASTUS, ASPARAGUS OFFICINALIS, AVENA SATIVA, CADMIUM METALLICUM, DAMIANA, GLANDULA SUPRARENALIS SUIS, JUNIPERUS COMMUNIS, LYCOPODIUM CLAVATUM, ORCHITINUM (BOVINE), PETROSELINUM SATIVUM, PITUITARUM POSTERIUM (BOVINE), PULSATILLA (VULGARIS), SABAL SERRULATA, SARSAPARILLA (SMILAX REGELII)	Energetix Corporation	ece117c4-5116-458e-888a-5ff3cf0cfbfb	2025-12-22	Warnings	Exact identifier ndc (package): 64578-0099-1 ndc (product): 64578-0099 ndc11 (package): 64578009901

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.