NDC11 73581040201

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
73581-0402-01	73581-0402
73581-0402-1	73581-0402
73581-402-01	73581-402

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
MUCUS RELIEF GUAIFENESIN EXTENDED-RELEASE 1200 mg	GUAIFENESIN	YYBA CORP	d9d2539b-bd31-66bd-e053-2a95a90aa583	2025-11-27	Warnings	Exact identifier ndc (package): 73581-402-01 ndc (product): 73581-402 ndc11 (package): 73581040201

Reported adverse events (FAERS/openFDA)#

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