Torsemide
Torsemide Tablets Rx only
Approved
Approval ID
c7f3a3f5-3ad6-45b7-af46-b75a2ce34769
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 19, 2013
Manufacturers
FDA
Carilion Materials Management
DUNS: 079239644
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Torsemide
Product Details
FDA regulatory identification and product classification information
FDA Identifiers
NDC Product Code68151-2946
Application NumberANDA079234
Product Classification
M
Marketing Category
C73584
G
Generic Name
Torsemide
Product Specifications
Route of AdministrationORAL
Effective DateOctober 3, 2012
FDA Product Classification
INGREDIENTS (6)
TORSEMIDEActive
Quantity: 5 mg in 1 1
Code: W31X2H97FB
Classification: ACTIB
POVIDONESInactive
Code: FZ989GH94E
Classification: IACT
CELLULOSE, MICROCRYSTALLINEInactive
Code: OP1R32D61U
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
CROSPOVIDONEInactive
Code: 68401960MK
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT