NDC 0378-1066 - Meloxicam

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
0378-1066
Manufacturer
ReadyMeds
Effective date
2014-07-01
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Meloxicam - ReadyMedsReadyMeds2014-07-01HUMAN PRESCRIPTION DRUG LABEL

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0378-1066-01EA - Each0378-1066473e1792-ed54-4097-a921-b3b34370e81412012-07-24
0378-1066-05EA - Each0378-1066034932ef-955a-4eaf-81ec-b494895831bf12012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MELOXICAMACTIVE INGREDIENTVG2QF83CGLMELOXICAM TABLET [READYMEDS]4
MELOXICAMACTIVE MOIETYVG2QF83CGLMELOXICAM TABLET [READYMEDS]4
CELLULOSE, MICROCRYSTALLINEINACTIVE INGREDIENTOP1R32D61UMELOXICAM TABLET [READYMEDS]4
CROSPOVIDONEINACTIVE INGREDIENT68401960MKMELOXICAM TABLET [READYMEDS]4
LACTOSE MONOHYDRATEINACTIVE INGREDIENTEWQ57Q8I5XMELOXICAM TABLET [READYMEDS]4
MAGNESIUM STEARATEINACTIVE INGREDIENT70097M6I30MELOXICAM TABLET [READYMEDS]4
SILICON DIOXIDEINACTIVE INGREDIENTETJ7Z6XBU4MELOXICAM TABLET [READYMEDS]4
SODIUM LAURYL SULFATEINACTIVE INGREDIENT368GB5141JMELOXICAM TABLET [READYMEDS]4