Product NDC: | 55154-2094 |
Proprietary Name: | Benztropine Mesylate |
Non Proprietary Name: | Benztropine Mesylate |
Active Ingredient(s): | 1 mg/1 & nbsp; Benztropine Mesylate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55154-2094 |
Labeler Name: | Cardinal Health |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA040742 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100114 |
Package NDC: | 55154-2094-0 |
Package Description: | 10 BLISTER PACK in 1 BAG (55154-2094-0) > 1 TABLET in 1 BLISTER PACK |
NDC Code | 55154-2094-0 |
Proprietary Name | Benztropine Mesylate |
Package Description | 10 BLISTER PACK in 1 BAG (55154-2094-0) > 1 TABLET in 1 BLISTER PACK |
Product NDC | 55154-2094 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Benztropine Mesylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20100114 |
Marketing Category Name | ANDA |
Labeler Name | Cardinal Health |
Substance Name | BENZTROPINE MESYLATE |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA] |