NDC11 51672215104

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
51672-2151-04	51672-2151
51672-2151-4	51672-2151

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
Minoxidil Topical Solution, 5%	MINOXIDIL SOLUTION	Sun Pharmaceutical Industries, Inc.	acc5ad74-4558-4be9-aab4-94ad9ddad6b2	2026-03-04	Warnings	Exact identifier ndc (package): 51672-2151-4 ndc (product): 51672-2151 ndc11 (package): 51672215104

Reported adverse events (FAERS/openFDA)#

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