NDC11 63323050701

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
63323-0507-01	63323-0507
63323-0507-1	63323-0507
63323-507-01	63323-507

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
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	12714f80-d6e5-4453-b66c-62f57c16ddfc	2021-03-12	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-507
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	7a68d899-2678-43a9-a9c1-ef8f916b562f	2021-03-10	Warnings, Adverse reactions	Exact identifier ndc (product): 63323-507
Meropenem	MEROPENEM	Fresenius Kabi USA, LLC	185181e3-c004-4d61-b992-5df94fe57a90	2020-10-19	Warnings, Adverse reactions	Exact identifier ndc (package): 63323-507-01 ndc (product): 63323-507 ndc11 (package): 63323050701

Reported adverse events (FAERS/openFDA)#

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