Eldepryl - selegiline hydrochloride
Navigation: NDC > Supplier starting with: S > SOMERSET PHARMACEUTICALS INC.| Field | Value |
|---|---|
| NDC Code: | 39506-022 |
| Proprietary Name: | Eldepryl |
| Suffix: | |
| Non-Proprietary Name: | selegiline hydrochloride |
| Dosage Form: | CAPSULE |
| Method: | ORAL |
| Original Marketing Date: | 15-05-1996 |
| End of Marketing: | 31-01-2014 |
| Category Name: | ANDA |
| Application Number: | ANDA020647 |
| Labeler: | SOMERSET PHARMACEUTICALS INC. |
| Substance Name: | SELEGILINE HYDROCHLORIDE |
| Active Numerator Strength: | 5 |
| Active Ingredient Unit: | mg/1 |
| Pharm Classes: | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA] |
| DEA Schedule: |