Product NDC: | 51991-793 |
Proprietary Name: | Rivastigmine Tartrate |
Non Proprietary Name: | Rivastigmine Tartrate |
Active Ingredient(s): | 1.5 mg/1 & nbsp; Rivastigmine Tartrate |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 51991-793 |
Labeler Name: | Breckenridge Pharmaceutical, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA091689 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120613 |
Package NDC: | 51991-793-10 |
Package Description: | 1000 CAPSULE in 1 BOTTLE (51991-793-10) |
NDC Code | 51991-793-10 |
Proprietary Name | Rivastigmine Tartrate |
Package Description | 1000 CAPSULE in 1 BOTTLE (51991-793-10) |
Product NDC | 51991-793 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Rivastigmine Tartrate |
Dosage Form Name | CAPSULE |
Route Name | ORAL |
Start Marketing Date | 20120613 |
Marketing Category Name | ANDA |
Labeler Name | Breckenridge Pharmaceutical, Inc |
Substance Name | RIVASTIGMINE TARTRATE |
Strength Number | 1.5 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA] |