NDC11 51672135802

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
51672-1358-02	51672-1358
51672-1358-2	51672-1358

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Clofenax	DICLOFENAC SODIUM, KINESIOLOGY TAPE	PureTek Corporation	b60e6572-0624-40c5-e053-2995a90ade48	2026-07-24	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51672-1358-2 ndc11 (package): 51672135802
Diclofenac Sodium	DICLOFENAC SODIUM	Sun Pharmaceutical Industries, Inc.	fae53d24-acf1-4250-888d-b8d965ffc3d3	2026-02-18	Boxed warning, Warnings, Adverse reactions	Exact identifier ndc (package): 51672-1358-2 ndc (product): 51672-1358 ndc11 (package): 51672135802

Reported adverse events (FAERS/openFDA)#

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