| NDC Code | 72319-021-02 |
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| Package Description | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72319-021-02) |
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| Product NDC | 72319-021 |
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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 | 20220615 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA213517 |
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| Manufacturer | i3 Pharmaceuticals, LLC |
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| Substance Name | RANOLAZINE |
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| Strength | 500 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Anti-anginal [EPC], Cytochrome P450 2D6 Inhibitors [MoA], Cytochrome P450 3A Inhibitors [MoA], Organic Cation Transporter 2 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA] |
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