Product NDC: | 53808-0740 |
Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Non Proprietary Name: | AMOXICILLIN AND CLAVULANATE POTASSIUM |
Active Ingredient(s): | 875; 125 mg/1; mg/1 & nbsp; AMOXICILLIN AND CLAVULANATE POTASSIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 53808-0740 |
Labeler Name: | State of Florida DOH Central Pharmacy |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065093 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090701 |
Package NDC: | 53808-0740-1 |
Package Description: | 30 DOSE PACK in 1 CARTON (53808-0740-1) > 1 TABLET, FILM COATED in 1 DOSE PACK |
NDC Code | 53808-0740-1 |
Proprietary Name | Amoxicillin and Clavulanate Potassium |
Package Description | 30 DOSE PACK in 1 CARTON (53808-0740-1) > 1 TABLET, FILM COATED in 1 DOSE PACK |
Product NDC | 53808-0740 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | AMOXICILLIN AND CLAVULANATE POTASSIUM |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20090701 |
Marketing Category Name | ANDA |
Labeler Name | State of Florida DOH Central Pharmacy |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength Number | 875; 125 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |