NDC11 51316081639

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
51316-0816-39	51316-0816
51316-816-39	51316-816

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
ACID REDUCER	FAMOTIDINE	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	7e5f9492-1d58-47a3-aac6-c41c81b348d5	2026-08-03	Warnings	Exact identifier ndc (package): 51316-816-39 ndc (product): 51316-816 ndc11 (package): 51316081639

Reported adverse events (FAERS/openFDA)#

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