NDC11 47335041083

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
47335-0410-83	47335-0410
47335-410-83	47335-410

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
Sumatriptan and Naproxen Sodium	SUMATRIPTAN AND NAPROXEN SODIUM	Sun Pharmaceutical Industries, Inc.	96ed12a3-fa76-4afd-bee8-1ab19eb607f3	2025-10-30	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 47335-410-83 ndc (product): 47335-410 ndc11 (package): 47335041083

Reported adverse events (FAERS/openFDA)#

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