NDC11 51672131605

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
51672-1316-05	51672-1316
51672-1316-5	51672-1316

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
Alclometasone Dipropionate	ALCLOMETASONE DIPROPIONATE	Sun Pharmaceutical Industries, Inc.	3b0dccd6-dee1-49dd-8c6d-82df5c7ee36c	2025-08-13	Adverse reactions	Exact identifier ndc (package): 51672-1316-5 ndc (product): 51672-1316 ndc11 (package): 51672131605

Reported adverse events (FAERS/openFDA)#

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