| NDC Code | 0378-0509-91 |
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| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-0509-91) |
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| Product NDC | 0378-0509 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dalfampridine |
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| Non-Proprietary Name | Dalfampridine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20180910 |
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| End Marketing Date | 20220531 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022250 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | DALFAMPRIDINE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Potassium Channel Antagonists [MoA], Potassium Channel Blocker [EPC] |
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