| NDC Code | 53489-369-10 |
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| Package Description | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (53489-369-10) |
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| Product NDC | 53489-369 |
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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 | 20041102 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075896 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | FELODIPINE |
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| Strength | 5 |
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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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