| NDC Code | 0187-0453-03 |
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| Package Description | 1 POUCH in 1 CARTON (0187-0453-03) > 10 TABLET, ORALLY DISINTEGRATING in 1 POUCH |
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| Product NDC | 0187-0453 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Zelapar |
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| Non-Proprietary Name | Selegiline Hydrochloride |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20060614 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021479 |
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| Manufacturer | Valeant Pharmaceuticals North America LLC |
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| Substance Name | SELEGILINE HYDROCHLORIDE |
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| Strength | 1.25 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Monoamine Oxidase Inhibitor [EPC],Monoamine Oxidase Inhibitors [MoA],Monoamine Oxidase Type B Inhibitor [EPC],Monoamine Oxidase-B Inhibitors [MoA] |
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