NDC Code | 72508-204-07 |
Package Description | 75 mL in 1 BOTTLE (72508-204-07) |
Product NDC | 72508-204 |
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 | 20190301 |
End Marketing Date | 20211001 |
Marketing Category Name | NDA |
Application Number | NDA050575 |
Manufacturer | Neopharma Inc |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength | 250; 62.5 |
Strength Unit | mg/5mL; mg/5mL |
Pharmacy Classes | Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |