Meloxicam
These highlights do not include all the information needed to use meloxicam safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USPInitial U.S. Approval: 2000
Approved
Approval ID
3d3b548c-005e-40b0-98d0-443cf08fdcde
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jun 8, 2011
Manufacturers
FDA
Blenheim Pharmacal, Inc.
DUNS: 171434587
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Meloxicam
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code10544-251
Application NumberANDA077944
Product Classification
M
Marketing Category
C73584
G
Generic Name
Meloxicam
Product Specifications
Route of AdministrationORAL
Effective DateJune 8, 2011
FDA Product Classification
INGREDIENTS (8)
MELOXICAMActive
Quantity: 15 mg in 1 1
Code: VG2QF83CGL
Classification: ACTIB
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
POVIDONEInactive
Code: FZ989GH94E
Classification: IACT
SODIUM CITRATEInactive
Code: 1Q73Q2JULR
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
COLLOIDAL SILICON DIOXIDEInactive
Code: ETJ7Z6XBU4
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT