NDC11 47335038261

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
47335-0382-61	47335-0382
47335-382-61	47335-382

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	Sun Pharmaceutical Industries, Inc.	f16beb64-5878-486a-82ee-8e83e728f26c	2021-11-08	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 47335-382-61 ndc (product): 47335-382 ndc11 (package): 47335038261

Reported adverse events (FAERS/openFDA)#

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