NDC 58980-610 - NOXIPAK

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
58980-610
Package NDCs from labels
58980-610-30
Manufacturer
SOLUTECH PHARMACEUTICALS LLC
Effective date
2017-11-08
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
NOXIPAK - SOLUTECH PHARMACEUTICALS LLCSOLUTECH PHARMACEUTICALS LLC2017-11-08HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58980-610-30NOXIPAK85 g in 1 TUBECREAM85 g17 g in 85g2
58980-610-30NOXIPAK1 in 1 BOXCREAM17 g in 85g2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58980-610NOXIPAK (FLUOCINOLONE ACETONIDE AND UREA) KIT [SOLUTECH PHARMACEUTICALS LLC]2Unmatched20171109_136cb37e-e939-40b5-9725-194b14a9b090.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
58980-610-30GM - Gram58980-6105b4999af-dec3-44ce-aa17-36b35674f8fb12012-07-24