| NDC Code | 45865-445-49 |
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| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (45865-445-49) |
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| Product NDC | 45865-445 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Felodipine |
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| Non-Proprietary Name | Felodipine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20101220 |
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| End Marketing Date | 20190630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090365 |
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| Manufacturer | Medsource Pharmaceuticals |
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| Substance Name | FELODIPINE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS] |
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