| NDC Code | 60687-792-01 |
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| Package Description | 100 BLISTER PACK in 1 CARTON (60687-792-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-792-11) |
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| Product NDC | 60687-792 |
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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 | 20240609 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA091569 |
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| Manufacturer | American Health Packaging |
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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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