NDC11 58657048707

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
58657-0487-07	58657-0487
58657-0487-7	58657-0487
58657-487-07	58657-487

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
Urea 40 Percent	UREA	Method Pharmaceuticals, LLC	d35b75e1-937d-ebc4-e053-2a95a90ac0d8	2026-02-12	Warnings, Adverse reactions	Exact identifier ndc (package): 58657-487-07 ndc (product): 58657-487 ndc11 (package): 58657048707

Reported adverse events (FAERS/openFDA)#

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