31722-531 NDC - TORSEMIDE

Drug Information

Product NDC: 31722-531

Proprietary Name: Torsemide

Non Proprietary Name: Torsemide

Active Ingredient(s):
  • 20 mg/1 TORSEMIDE


Administration Route(s): ORAL

Dosage Form(s): TABLET

Pharmacy Class(es):
  • Increased Diuresis at Loop of Henle [PE];
  • Loop Diuretic [EPC]

Labeler Information

Labeler Name: Camber Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA079234
Marketing Category: ANDA
Start Marketing Date:1/1/2011

Package Information

No. Package Code Package Description Billing Unit
131722-531-01100 TABLET in 1 BOTTLE (31722-531-01)EA
231722-531-05500 TABLET in 1 BOTTLE (31722-531-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC31722-531The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN PRESCRIPTION DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMETorsemideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMETorsemideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLETThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/1/2011The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
MARKETING CATEGORY NAMEANDAIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
APPLICATION NUMBERANDA079234The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
LABELER NAMECamber Pharmaceuticals, Inc.The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
SUBSTANCE NAMETORSEMIDEThe translation of the dosage form Code submitted by the firm.
ACTIVE NUMERATOR STRENGTH20 
ACTIVE INGRED UNITmg/1 
PHARM CLASSESIncreased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC] 

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This page was last updated on: 2/1/2023