NDC11 66220071901

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
66220-0719-01	66220-0719
66220-0719-1	66220-0719
66220-719-01	66220-719

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 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
KRISTALOSE	LACTULOSE	Cumberland Pharmaceuticals Inc.	535dd1ea-b567-49f7-9a84-8ea91e78c466	2018-09-17	Warnings, Adverse reactions	Exact identifier ndc (package): 66220-719-01 ndc (product): 66220-719 ndc11 (package): 66220071901

Reported adverse events (FAERS/openFDA)#

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