NDC Code | 24555-1852-3 |
Package Description | 30 TABLET, FILM COATED in 1 BLISTER PACK (24555-1852-3) |
Product NDC | 24555-1852 |
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 | 20240205 |
Marketing Category Name | ANDA |
Application Number | ANDA065063 |
Manufacturer | Correct Rx Pharmacy Services, 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] |