NDC11 72266011801

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
72266-0118-01	72266-0118
72266-0118-1	72266-0118
72266-118-01	72266-118

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
Ketorocaine LM Kit	KETOROLAC TROMETHAMINE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE	Asclemed USA, Inc.	35ffe071-8bc1-4c88-8c85-645847acf169	2026-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 72266-118-01 ndc11 (package): 72266011801
Ketorocaine L Kit	KETOROLAC TROMETHAMINE, LIDOCAINE HYDROCHLORIDE, POVIDINE IODINE	Asclemed USA, Inc.	ee0d396c-5caa-4a1a-9865-1a742d9d8d68	2026-01-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 72266-118-01 ndc11 (package): 72266011801
ketorolac tromethamine	KETOROLAC TROMETHAMINE	FOSUN PHARMA USA INC	1aae6a4d-0909-4672-aa26-e3f2d8c4d413	2024-09-20	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 72266-118-01 ndc (product): 72266-118 ndc11 (package): 72266011801

Reported adverse events (FAERS/openFDA)#

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