Meloxicam
These highlights do not include all the information needed to use meloxicam safely and effectively. See full prescribing information for meloxicam tablets. Meloxicam Tablets, USP Initial U.S. Approval: 2000
Approved
Approval ID
3ba4c6e0-cb83-43b5-a623-1f2af9c2b07c
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Feb 18, 2013
Manufacturers
FDA
MedVantx, Inc.
DUNS: 806427725
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Meloxicam
PRODUCT DETAILS
NDC Product Code66116-392
Application NumberANDA078008
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateFebruary 18, 2013
Generic NameMeloxicam
INGREDIENTS (8)
SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MELOXICAMActive
Quantity: 7.5 mg in 1 1
Code: VG2QF83CGL
Classification: ACTIB
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
POVIDONE K25Inactive
Code: K0KQV10C35
Classification: IACT
TRISODIUM CITRATE DIHYDRATEInactive
Code: B22547B95K
Classification: IACT