NDC11 87069012364

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
87069-0123-64	87069-0123
87069-123-64	87069-123

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	Join
Leukotrap RC PL System	CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM	GVS TM INC	54eab581-bc48-f9f0-e063-6394a90a4b93	2026-06-25	Exact identifier ndc (package): 87069-123-64 ndc (product): 87069-123 ndc11 (package): 87069012364
Leukotrap RC PL System	CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM	GVS TM INC	54e9a497-7a94-44c9-e063-6294a90a84da	2026-06-23	Exact identifier ndc (product): 87069-123
Leukotrap RC PL System	CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM	GVS TM INC	54eb0462-cd00-4467-e063-6394a90aa371	2026-06-23	Exact identifier ndc (product): 87069-123

Reported adverse events (FAERS/openFDA)#

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