| NDC Code | 68788-8299-1 |
|---|
| Package Description | 125 mL in 1 BOTTLE (68788-8299-1) |
|---|
| Product NDC | 68788-8299 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Dosage Form | SUSPENSION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20221129 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065373 |
|---|
| Manufacturer | Preferred Pharmaceuticals Inc. |
|---|
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
|---|
| Strength | 600; 42.9 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
|---|