| NDC Code | 48792-7894-1 |
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| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (48792-7894-1) |
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| Product NDC | 48792-7894 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ranolazine |
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| Non-Proprietary Name | Ranolazine |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20200331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA211865 |
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| Manufacturer | Sunshine Lake Pharma Co., Ltd. |
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| Substance Name | RANOLAZINE |
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| Strength | 1000 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-anginal [EPC],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA],Cytochrome P450 2D6 Inhibitors [MoA],Organic Cation Transporter 2 Inhibitors [MoA] |
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