| NDC Code | 50090-2219-0 |
|---|
| Package Description | 125 mL in 1 BOTTLE (50090-2219-0) |
|---|
| Product NDC | 50090-2219 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Dosage Form | POWDER, FOR SUSPENSION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20111220 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA201091 |
|---|
| Manufacturer | A-S Medication Solutions |
|---|
| 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] |
|---|