| NDC Code | 48792-7817-1 |
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| Package Description | 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (48792-7817-1) |
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| Product NDC | 48792-7817 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Clarithromycin |
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| Non-Proprietary Name | Clarithromycin |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20150929 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203584 |
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| Manufacturer | Sunshine Lake Pharma Co., Ltd. |
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| Substance Name | CLARITHROMYCIN |
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| Strength | 250 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Macrolide Antimicrobial [EPC],Macrolides [Chemical/Ingredient],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA] |
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