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Trospium Chloride - 0574-0145-60 - (trospium chloride)

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Drug Information of Trospium Chloride

Product NDC: 0574-0145
Proprietary Name: Trospium Chloride
Non Proprietary Name: trospium chloride
Active Ingredient(s): 20    mg/1 & nbsp;   trospium chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Trospium Chloride

Product NDC: 0574-0145
Labeler Name: Paddock Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091573
Marketing Category: ANDA
Start Marketing Date: 20101117

Package Information of Trospium Chloride

Package NDC: 0574-0145-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (0574-0145-60)

NDC Information of Trospium Chloride

NDC Code 0574-0145-60
Proprietary Name Trospium Chloride
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (0574-0145-60)
Product NDC 0574-0145
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name trospium chloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101117
Marketing Category Name ANDA
Labeler Name Paddock Laboratories, Inc.
Substance Name TROSPIUM CHLORIDE
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Trospium Chloride


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