NDC Code | 60505-2539-5 |
Package Description | 500 TABLET in 1 BOTTLE (60505-2539-5) |
Product NDC | 60505-2539 |
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 | 20090706 |
Marketing Category Name | ANDA |
Application Number | ANDA065333 |
Manufacturer | Apotex Corp. |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength | 250; 125 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |