| NDC Code | 54868-5175-0 |
|---|
| Package Description | 100 mL in 1 BOTTLE (54868-5175-0) |
|---|
| Product NDC | 54868-5175 |
|---|
| 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 | 20050316 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065066 |
|---|
| Manufacturer | Physicians Total Care, Inc. |
|---|
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
|---|
| Strength | 400; 57 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
|---|