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Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 0143-9982-50 - (Amoxicillin and Clavulanate Potassium)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 0143-9982 |
| 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) |
Labeler Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 0143-9982 |
| Labeler Name: | West-ward Pharmaceutical Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065191 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20071201 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 0143-9982-50 |
| Package Description: | 50 mL in 1 BOTTLE (0143-9982-50) |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 0143-9982-50 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 50 mL in 1 BOTTLE (0143-9982-50) |
| Product NDC | 0143-9982 |
| 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 | 20071201 |
| Marketing Category Name | ANDA |
| Labeler Name | West-ward Pharmaceutical Corp |
| Substance Name | AMOXICILLIN; CLAVULANIC ACID |
| Strength Number | 400; 57 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
