NDC11 44911068301

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
44911-0683-01	44911-0683
44911-0683-1	44911-0683
44911-683-01	44911-683

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
Thyropar	FUCUS VESICULOSUS, SPONGIA TOSTA, GLANDULA SUPRARENALIS SUIS, HYPOPHYSIS SUIS, THYROIDINUM (SUIS), BROMIUM, CALCAREA CARBONICA, GRAPHITES, IODIUM, LACHESIS MUTUS, LEVOTHYROXINUM, PULSATILLA (PRATENSIS), SELENIUM METALLICUM	Energique, Inc.	fe5065b4-7332-44fc-843a-f24b1e7a44e7	2026-06-24	Warnings	Exact identifier ndc (package): 44911-0683-1 ndc (product): 44911-0683 ndc11 (package): 44911068301

Reported adverse events (FAERS/openFDA)#

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