NDC11 51316040763

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
51316-0407-63	51316-0407
51316-407-63	51316-407

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
COMPLETE ACID REDUCER	FAMOTIDINE, CALCIUM CARBONATE AND MAGNESIUM HYDROXIDE	CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED	962ced24-0fb3-4aba-b32e-2e6fa1c1c5d7	2026-07-22	Warnings	Exact identifier ndc (package): 51316-407-63 ndc (product): 51316-407 ndc11 (package): 51316040763

Reported adverse events (FAERS/openFDA)#

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