| NDC Code | 60505-2541-2 |
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| Package Description | 20 TABLET in 1 BOTTLE (60505-2541-2) |
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| Product NDC | 60505-2541 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Amoxicillin And Clavulanate Potassium |
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| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 20090706 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065317 |
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| Manufacturer | Apotex Corp. |
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| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
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| Strength | 875; 125 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
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