| NDC Code | 0093-7446-56 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0093-7446-56) |
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| Product NDC | 0093-7446 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Fluvastatin Sodium |
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| Non-Proprietary Name | Fluvastatin Sodium |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160602 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079011 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | FLUVASTATIN SODIUM |
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| Strength | 80 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA] |
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