Product NDC: | 0143-9853 |
Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Non Proprietary Name: | Amoxicillin and Clavulanate Potassium |
Active Ingredient(s): | 600; 42.9 mg/5mL; mg/5mL & nbsp; Amoxicillin and Clavulanate Potassium |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0143-9853 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA065373 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090803 |
Package NDC: | 0143-9853-75 |
Package Description: | 75 mL in 1 BOTTLE (0143-9853-75) |
NDC Code | 0143-9853-75 |
Proprietary Name | Amoxicillin and Clavulanate Potassium |
Package Description | 75 mL in 1 BOTTLE (0143-9853-75) |
Product NDC | 0143-9853 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Amoxicillin and Clavulanate Potassium |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20090803 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
Strength Number | 600; 42.9 |
Strength Unit | mg/5mL; mg/5mL |
Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |