NDC Code | 68788-9725-4 |
Package Description | 14 TABLET, FILM COATED in 1 BOTTLE (68788-9725-4) |
Product NDC | 68788-9725 |
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 | 20121119 |
Marketing Category Name | ANDA |
Application Number | ANDA091569 |
Manufacturer | Preferred Pharmaceuticals, 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] |