| NDC Code | 0093-8675-74 |
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| Package Description | 200 mL in 1 BOTTLE (0093-8675-74) |
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| Product NDC | 0093-8675 |
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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 | 20040923 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065162 |
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| Manufacturer | Teva Pharmaceuticals USA, Inc. |
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| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
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| Strength | 600; 42.9 |
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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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