Product NDC: | 21695-546 |
Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Non Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Active Ingredient(s): | 400; 57 mg/5mL; mg/5mL & nbsp; Amoxicillin and Clavulanate Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | POWDER, FOR SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-546 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065066 |
Marketing Category: | ANDA |
Start Marketing Date: | 20020605 |
Package NDC: | 21695-546-00 |
Package Description: | 100 mL in 1 BOTTLE (21695-546-00) |
NDC Code | 21695-546-00 |
Proprietary Name | Amoxicillin and Clavulanate Potassium |
Package Description | 100 mL in 1 BOTTLE (21695-546-00) |
Product NDC | 21695-546 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amoxicillin and Clavulanate Potassium |
Dosage Form Name | POWDER, FOR SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20020605 |
Marketing Category Name | ANDA |
Labeler Name | Rebel Distributors Corp. |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength Number | 400; 57 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |