NDC11 67877062605

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
67877-0626-05	67877-0626
67877-0626-5	67877-0626
67877-626-05	67877-626

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
Ibuprofen and famotidine	IBUPROFEN AND FAMOTIDINE	Ascend Laboratories, LLC	4493d4cd-ca8e-4b0a-9b65-b75e55bf8b9e	2026-07-28	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 67877-626-05 ndc (product): 67877-626 ndc11 (package): 67877062605

Reported adverse events (FAERS/openFDA)#

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