| NDC Code | 70518-2189-0 |
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| Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2189-0) |
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| Product NDC | 70518-2189 |
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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, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20190708 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065117 |
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| Manufacturer | REMEDYREPACK INC. |
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| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
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| Strength | 500; 125 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
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