Product NDC: | 60505-3454 |
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 |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 60505-3454 |
Labeler Name: | Apotex Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091513 |
Marketing Category: | ANDA |
Start Marketing Date: | 20121015 |
Package NDC: | 60505-3454-6 |
Package Description: | 60 TABLET in 1 BOTTLE (60505-3454-6) |
NDC Code | 60505-3454-6 |
Proprietary Name | TROSPIUM CHLORIDE |
Package Description | 60 TABLET in 1 BOTTLE (60505-3454-6) |
Product NDC | 60505-3454 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | TROSPIUM CHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20121015 |
Marketing Category Name | ANDA |
Labeler Name | Apotex Corp. |
Substance Name | TROSPIUM CHLORIDE |
Strength Number | 20 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA] |