| Product NDC: | 64980-112 |
| 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: | 64980-112 |
| Labeler Name: | Rising Pharmaceuticals Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA072265 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20020813 |
| Package NDC: | 64980-112-01 |
| Package Description: | 100 TABLET in 1 BOTTLE, PLASTIC (64980-112-01) |
| NDC Code | 64980-112-01 |
| Proprietary Name | BENZTROPINE MESYLATE |
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (64980-112-01) |
| Product NDC | 64980-112 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | BENZTROPINE MESYLATE |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20020813 |
| Marketing Category Name | ANDA |
| Labeler Name | Rising Pharmaceuticals Inc |
| Substance Name | BENZTROPINE MESYLATE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Anticholinergic [EPC],Antihistamine [EPC],Cholinergic Antagonists [MoA],Histamine Receptor Antagonists [MoA] |