| NDC Code | 68788-8355-2 |
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| Package Description | 20 TABLET in 1 BOTTLE (68788-8355-2) |
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| Product NDC | 68788-8355 |
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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 | 20230210 |
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| End Marketing Date | 20250101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203824 |
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| Manufacturer | Preferred Pharmaceuticals Inc. |
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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 [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
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