| NDC Code | 61919-202-20 |
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| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (61919-202-20) |
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| Product NDC | 61919-202 |
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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 | 20150101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091568 |
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| Manufacturer | DirectRX |
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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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