NDC11 83324033712

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
83324-0337-12	83324-0337
83324-337-12	83324-337

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
QUALITY CHOICE ULTRA STRENGTH STOMACH RELIEF	BISMUTH SUBSALICYLATE	QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)	67c610b1-fe94-4ad3-ad1a-8bd93a4da9d9	2025-09-11	Warnings	Exact identifier ndc (package): 83324-337-12 ndc (product): 83324-337 ndc11 (package): 83324033712

Reported adverse events (FAERS/openFDA)#

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