| NDC Code | 70518-2082-0 |
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| Package Description | 75 mL in 1 BOTTLE (70518-2082-0) |
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| Product NDC | 70518-2082 |
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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 | POWDER, FOR SUSPENSION |
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| Usage | ORAL |
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| Start Marketing Date | 20190515 |
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| Marketing Category Name | NDA |
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| Application Number | NDA050725 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
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| Strength | 250; 62.5 |
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| Strength Unit | mg/5mL; mg/5mL |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
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