NDC Code | 68071-3107-3 |
Package Description | 3 TABLET, FILM COATED in 1 BOTTLE (68071-3107-3) |
Product NDC | 68071-3107 |
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 | 20021031 |
Marketing Category Name | ANDA |
Application Number | ANDA065101 |
Manufacturer | NuCare 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] |