NDC11 63323032112

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
63323-0321-12	63323-0321
63323-321-12	63323-321

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
POLYMYXIN B	POLYMYXIN B SULFATE	Fresenius Kabi USA, LLC	704a41f5-b109-4c16-8d3e-1495c9917952	2021-05-31	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 63323-321-12 ndc (product): 63323-321 ndc11 (package): 63323032112
POLYMYXIN B	POLYMYXIN B SULFATE	Fresenius Kabi USA, LLC	fbc12c18-567b-41bc-89d0-efd29616615c	2021-02-28	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-321

Reported adverse events (FAERS/openFDA)#

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