| Product NDC: | 60505-3223 |
| Proprietary Name: | Rivastigmine Tartrate |
| Non Proprietary Name: | Rivastigmine Tartrate |
| Active Ingredient(s): | 6 mg/1 & nbsp; Rivastigmine Tartrate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 60505-3223 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA091072 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130220 |
| Package NDC: | 60505-3223-3 |
| Package Description: | 30 CAPSULE in 1 BOTTLE (60505-3223-3) |
| NDC Code | 60505-3223-3 |
| Proprietary Name | Rivastigmine Tartrate |
| Package Description | 30 CAPSULE in 1 BOTTLE (60505-3223-3) |
| Product NDC | 60505-3223 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Rivastigmine Tartrate |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130220 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | RIVASTIGMINE TARTRATE |
| Strength Number | 6 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |