| NDC Code | 66685-1011-0 |
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| Package Description | 50 mL in 1 BOTTLE (66685-1011-0) |
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| Product NDC | 66685-1011 |
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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 | 20040813 |
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| End Marketing Date | 20250531 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065098 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
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| Strength | 200; 28.5 |
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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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