Product NDC: | 68546-229 |
Proprietary Name: | AZILECT |
Non Proprietary Name: | rasagiline mesylate |
Active Ingredient(s): | 1 mg/1 & nbsp; rasagiline mesylate |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68546-229 |
Labeler Name: | Teva Neuroscience, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021641 |
Marketing Category: | NDA |
Start Marketing Date: | 20090609 |
Package NDC: | 68546-229-27 |
Package Description: | 1 BLISTER PACK in 1 CARTON (68546-229-27) > 7 TABLET in 1 BLISTER PACK |
NDC Code | 68546-229-27 |
Proprietary Name | AZILECT |
Package Description | 1 BLISTER PACK in 1 CARTON (68546-229-27) > 7 TABLET in 1 BLISTER PACK |
Product NDC | 68546-229 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | rasagiline mesylate |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090609 |
Marketing Category Name | NDA |
Labeler Name | Teva Neuroscience, Inc. |
Substance Name | RASAGILINE MESYLATE |
Strength Number | 1 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA] |