NDC11 82442054671

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
82442-0546-71	82442-0546
82442-546-71	82442-546

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
Up and Up Dual Action Acid Reducer and Antacid	FAMOTIDINE, CALCIUM CARBONATE, MAGNESIUM HYDROXIDE	Target Corporation	2f020677-77a0-4e13-9397-e9deeda63293	2025-09-10	Warnings	Exact identifier ndc (package): 82442-546-71 ndc (product): 82442-546 ndc11 (package): 82442054671

Reported adverse events (FAERS/openFDA)#

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