NDC11 63323064907

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
63323-0649-07	63323-0649
63323-0649-7	63323-0649
63323-649-07	63323-649

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
Levothyroxine Sodium	LEVOTHYROXINE SODIUM ANHYDROUS	Fresenius Kabi USA, LLC	ce990712-49c1-4f66-9ee4-c770e8ec394c	2025-04-17	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 63323-649-07 ndc (product): 63323-649 ndc11 (package): 63323064907
Levothyroxine Sodium	LEVOTHYROXINE SODIUM ANHYDROUS	Fresenius Kabi USA, LLC	152d071f-d4aa-46d2-b397-61c1cabdd86d	2024-10-14	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-649
Levothyroxine Sodium	LEVOTHYROXINE SODIUM ANHYDROUS	Fresenius Kabi USA, LLC	f88f44d8-2f18-4155-9d78-6323d19fbafe	2024-10-14	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-649

Reported adverse events (FAERS/openFDA)#

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