| NDC Code | 70518-2189-1 |
|---|
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (70518-2189-1) |
|---|
| Product NDC | 70518-2189 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Non-Proprietary Name | Amoxicillin And Clavulanate Potassium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190708 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065117 |
|---|
| Manufacturer | REMEDYREPACK INC. |
|---|
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
|---|
| Strength | 500; 125 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |
|---|