NDC11 45802011222

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
45802-0112-22	45802-0112
45802-112-22	45802-112

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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
DermacinRx Clorhexacin	MUPIROCIN OINTMENT	PureTek Corporation	3c8cb9a6-58e5-4e8d-bfdc-1432a1bde6f9	2024-12-13	Warnings, Adverse reactions	Exact identifier ndc (package): 45802-112-22 ndc11 (package): 45802011222
mupirocin	MUPIROCIN	Padagis Israel Pharmaceuticals Ltd	e9b61f01-3c67-42a4-a62b-10f1d1343190	2023-12-31	Warnings, Adverse reactions	Exact identifier ndc (package): 45802-112-22 ndc (product): 45802-112 ndc11 (package): 45802011222

Reported adverse events (FAERS/openFDA)#

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