Rasagiline is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Teva Pharmaceuticals Usa, Inc.. The primary component is Rasagiline Mesylate.
Product ID | 0093-3061_0c7edeb7-f1a4-4fa0-afed-6e037f785ed4 |
NDC | 0093-3061 |
Product Type | Human Prescription Drug |
Proprietary Name | Rasagiline |
Generic Name | Rasagiline |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2017-01-03 |
Marketing Category | NDA AUTHORIZED GENERIC / NDA AUTHORIZED GENERIC |
Application Number | NDA021641 |
Labeler Name | Teva Pharmaceuticals USA, Inc. |
Substance Name | RASAGILINE MESYLATE |
Active Ingredient Strength | 1 mg/1 |
Pharm Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |
Marketing Start Date | 2017-01-03 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA021641 |
Product Type | HUMAN PRESCRIPTION DRUG |
Billing Unit | EA |
Marketing Start Date | 2017-01-03 |
Ingredient | Strength |
---|---|
RASAGILINE MESYLATE | 1 mg/1 |
SPL SET ID: | e802c83c-e581-4a11-b83d-1df47120078d |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |
NDC | Brand Name | Generic Name |
---|---|---|
0093-3060 | Rasagiline | Rasagiline |
0093-3061 | Rasagiline | Rasagiline |
16714-770 | Rasagiline | Rasagiline |
16714-771 | Rasagiline | Rasagiline |
42291-779 | Rasagiline | Rasagiline |
42291-780 | Rasagiline | Rasagiline |
42571-220 | RASAGILINE | Rasagiline |
42571-221 | RASAGILINE | Rasagiline |
47781-683 | Rasagiline | Rasagiline |
47781-690 | Rasagiline | Rasagiline |
67877-259 | Rasagiline | Rasagiline |
67877-260 | Rasagiline | Rasagiline |