NDC Code | 70518-2225-6 |
Package Description | 100 POUCH in 1 BOX (70518-2225-6) / 1 TABLET, FILM COATED in 1 POUCH (70518-2225-7) |
Product NDC | 70518-2225 |
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 | 20190719 |
Marketing Category Name | ANDA |
Application Number | ANDA091568 |
Manufacturer | REMEDYREPACK INC. |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength | 875; 125 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA] |