| NDC Code | 60505-2539-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (60505-2539-3) |
|---|
| 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] |
|---|