NDC11 85534005203

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
85534-0052-03	85534-0052
85534-0052-3	85534-0052
85534-052-03	85534-052

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
Duloxetine	DULOXETINE	HAWAII REPACK, INC.	79bfd6be-a1ff-4786-b4e2-abbd0a3e3932	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 85534-0052-3 ndc (product): 85534-0052 ndc11 (package): 85534005203

Reported adverse events (FAERS/openFDA)#

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