NDC11 63323001341

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
63323-0013-41	63323-0013
63323-013-41	63323-013

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 · 3 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Thiamine	THIAMINE HYDROCHLORIDE	Fresenius Kabi USA, LLC	c3c9db74-95d4-487c-90c3-c810786fbaec	2026-01-14	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-013
Thiamine	THIAMINE HYDROCHLORIDE	Fresenius Kabi USA, LLC	ca4899c6-cea1-48d6-b0ae-9efcf67f6fcb	2026-01-13	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-013
Thiamine	THIAMINE HYDROCHLORIDE	Fresenius Kabi USA, LLC	af3f9344-f743-4bad-b319-53b96e13fee2	2026-01-09	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-013-41 ndc (product): 63323-013 ndc11 (package): 63323001341

Reported adverse events (FAERS/openFDA)#

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