FDA.reportPublic FDA data

NDC11 59088044207

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 NDCProduct root
59088-0442-0759088-0442
59088-0442-759088-0442
59088-442-0759088-442

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 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
MiconatateMICONAZOLE NITRATE AND TOLNAFTATEPureTek Corporationc45c8f8f-9042-a428-e053-2a95a90acda92024-10-16WarningsExact identifier
ndc (package): 59088-442-07
ndc11 (package): 59088044207
Mycozyl APMICONAZOLE NITRATEPureTek Corporationb3c46a30-7ff2-0dc4-e053-2995a90aa5712024-10-01WarningsExact identifier
ndc (package): 59088-442-07
ndc (product): 59088-442
ndc11 (package): 59088044207

Reported adverse events (FAERS/openFDA)#

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