NDC Code | 68788-7805-2 |
Package Description | 20 TABLET in 1 BOTTLE (68788-7805-2) |
Product NDC | 68788-7805 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amoxicillin And Clavulanate Potassium |
Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20201028 |
Marketing Category Name | ANDA |
Application Number | ANDA203824 |
Manufacturer | Preferred Pharmaceuticals Inc. |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength | 875; 125 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |