| NDC Code | 81964-212-03 |
|---|
| Package Description | 100 mL in 1 BOTTLE (81964-212-03) |
|---|
| Product NDC | 81964-212 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Dosage Form | FOR SUSPENSION |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20221205 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA050575 |
|---|
| Manufacturer | USAntibiotics, LLC |
|---|
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
|---|
| Strength | 125; 31.25 |
|---|
| Strength Unit | mg/5mL; mg/5mL |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
|---|