NDC11 58602072902

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
58602-0729-02	58602-0729
58602-0729-2	58602-0729
58602-729-02	58602-729

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	OMEPRAZOLE	Aurohealth LLC	fde12bf8-3e3b-4813-a8c4-4385e7de8204	2024-06-14	Warnings	Exact identifier ndc (package): 58602-729-02 ndc (product): 58602-729 ndc11 (package): 58602072902

Reported adverse events (FAERS/openFDA)#

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