Product NDC: | 54569-5689 |
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: | 54569-5689 |
Labeler Name: | A-S Medication Solutions LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050575 |
Marketing Category: | NDA |
Start Marketing Date: | 19901022 |
Package NDC: | 54569-5689-0 |
Package Description: | 50 mL in 1 BOTTLE (54569-5689-0) |
NDC Code | 54569-5689-0 |
Proprietary Name | amoxicillin and clavulanate potassium |
Package Description | 50 mL in 1 BOTTLE (54569-5689-0) |
Product NDC | 54569-5689 |
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 | 19901022 |
Marketing Category Name | NDA |
Labeler Name | A-S Medication Solutions LLC |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength Number | 400; 57 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |