| NDC Code | 62135-462-20 |
|---|
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (62135-462-20) |
|---|
| Product NDC | 62135-462 |
|---|
| 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 | 20220801 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA065064 |
|---|
| Manufacturer | Chartwell RX, LLC |
|---|
| 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] |
|---|