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Trospium Chloride - 68462-461-30 - (Trospium Chloride)

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Drug Information of Trospium Chloride

Product NDC: 68462-461
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: 68462-461
Labeler Name: Glenmark Generics Inc., USA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091575
Marketing Category: ANDA
Start Marketing Date: 20100813

Package Information of Trospium Chloride

Package NDC: 68462-461-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (68462-461-30)

NDC Information of Trospium Chloride

NDC Code 68462-461-30
Proprietary Name Trospium Chloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (68462-461-30)
Product NDC 68462-461
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Trospium Chloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100813
Marketing Category Name ANDA
Labeler Name Glenmark Generics Inc., USA
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


General Information