NDC11 82009003010

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
82009-0030-10	82009-0030
82009-030-10	82009-030

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 HYDROCHLORIDE	Quallent Pharmaceuticals Health, LLC	31362045-201f-45f3-99f2-a5e322a0c30b	2025-11-03	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 82009-030-10 ndc (product): 82009-030 ndc11 (package): 82009003010

Reported adverse events (FAERS/openFDA)#

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