Selegiline Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by I3 Pharmaceuticals, Llc. The primary component is Selegiline Hydrochloride.
Product ID | 72319-006_c81e983b-455e-2e65-e053-2a95a90a3123 |
NDC | 72319-006 |
Product Type | Human Prescription Drug |
Proprietary Name | Selegiline Hydrochloride |
Generic Name | Selegiline Hydrochloride |
Dosage Form | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 2021-07-30 |
Marketing Category | ANDA / |
Application Number | ANDA074672 |
Labeler Name | i3 Pharmaceuticals, LLC |
Substance Name | SELEGILINE HYDROCHLORIDE |
Active Ingredient Strength | 5 mg/1 |
Pharm Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA] |
NDC Exclude Flag | N |
Listing Certified Through | 2022-12-31 |
Marketing Start Date | 2021-07-30 |
NDC Exclude Flag | N |
Sample Package? | N |
NDC | Brand Name | Generic Name |
---|---|---|
0378-9290 | Selegiline Hydrochloride | selegiline hydrochloride |
10135-737 | Selegiline Hydrochloride | Selegiline Hydrochloride |
16571-659 | Selegiline Hydrochloride | Selegiline Hydrochloride |
50090-2918 | Selegiline Hydrochloride | Selegiline Hydrochloride |
51862-146 | Selegiline Hydrochloride | Selegiline Hydrochloride |
60429-019 | SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE |
60429-176 | Selegiline Hydrochloride | Selegiline Hydrochloride |
60505-0055 | SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE |
60505-3438 | Selegiline Hydrochloride | Selegiline Hydrochloride |
67253-700 | SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE |
68151-2649 | SELEGILINE HYDROCHLORIDE | SELEGILINE HYDROCHLORIDE |
70954-504 | Selegiline Hydrochloride | Selegiline Hydrochloride |
71205-888 | Selegiline Hydrochloride | Selegiline Hydrochloride |
72319-006 | Selegiline Hydrochloride | Selegiline Hydrochloride |
0187-0453 | ZELAPAR | SELEGILINE HYDROCHLORIDE |