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) |
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 NDC: | 68462-461-60 |
Package Description: | 60 TABLET, FILM COATED in 1 BOTTLE (68462-461-60) |
NDC Code | 68462-461-60 |
Proprietary Name | Trospium Chloride |
Package Description | 60 TABLET, FILM COATED in 1 BOTTLE (68462-461-60) |
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] |