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Selegiline Hydrochloride
Selegiline Hydrochloride - 60505-3438-8 - (Selegiline Hydrochloride)
Drug Information of Selegiline Hydrochloride
| Product NDC: | 60505-3438 |
| Proprietary Name: | Selegiline Hydrochloride |
| Non Proprietary Name: | Selegiline Hydrochloride |
| Active Ingredient(s): | 5 mg/1 & nbsp; Selegiline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Selegiline Hydrochloride
| Product NDC: | 60505-3438 |
| Labeler Name: | Apotex Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA074871 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970706 |
Package Information of Selegiline Hydrochloride
| Package NDC: | 60505-3438-8 |
| Package Description: | 500 TABLET in 1 BOTTLE (60505-3438-8) |
NDC Information of Selegiline Hydrochloride
| NDC Code | 60505-3438-8 |
| Proprietary Name | Selegiline Hydrochloride |
| Package Description | 500 TABLET in 1 BOTTLE (60505-3438-8) |
| Product NDC | 60505-3438 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Selegiline Hydrochloride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19970706 |
| Marketing Category Name | ANDA |
| Labeler Name | Apotex Corp. |
| Substance Name | SELEGILINE HYDROCHLORIDE |
| Strength Number | 5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA] |
