MedPath

Demadex

Approved
Approval ID

aff713e8-2cb6-4e49-94a2-c55c5491c822

Product Type

HUMAN PRESCRIPTION DRUG LABEL

Effective Date

Aug 4, 2009

Manufacturers
FDA

Physicians Total Care, Inc.

DUNS: 194123980

Products 2

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 Code54868-4687
Application NumberNDA020136
Product Classification
M
Marketing Category
C73594
G
Generic Name
Torsemide
Product Specifications
Route of AdministrationORAL
Effective DateNovember 6, 2009
FDA Product Classification

INGREDIENTS (1)

TORSEMIDEActive
Quantity: 20 mg in 1 1
Code: W31X2H97FB
Classification: ACTIB

Torsemide

Product Details

FDA regulatory identification and product classification information

FDA Identifiers
NDC Product Code54868-3835
Application NumberNDA020136
Product Classification
M
Marketing Category
C73594
G
Generic Name
Torsemide
Product Specifications
Route of AdministrationORAL
Effective DateNovember 6, 2009
FDA Product Classification

INGREDIENTS (1)

TORSEMIDEActive
Quantity: 10 mg in 1 1
Code: W31X2H97FB
Classification: ACTIB

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Demadex - FDA Drug Approval Details