NDC11 63323016226

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
63323-0162-26	63323-0162
63323-162-26	63323-162

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
Ketorolac Tromethamine	KETOROLAC TROMETHAMINE	Fresenius Kabi USA, LLC	d1920335-8e45-4960-b6e9-e6f1f9e6820c	2024-07-23	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-162
Ketorolac Tromethamine	KETOROLAC TROMETHAMINE	Fresenius Kabi USA, LLC	950b7295-3f68-4027-ac2b-2f7d0f5f8ef9	2022-11-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (product): 63323-162
Ketorolac Tromethamine	KETOROLAC TROMETHAMINE	Fresenius Kabi USA, LLC	ccf905ca-e164-4779-9485-2d139c821bad	2022-09-15	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 63323-162-26 ndc (product): 63323-162 ndc11 (package): 63323016226

Reported adverse events (FAERS/openFDA)#

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