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Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 66685-1011-0 - (amoxicillin and clavulanate potassium)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 66685-1011 |
| Proprietary Name: | Amoxicillin and Clavulanate Potassium |
| Non Proprietary Name: | amoxicillin and clavulanate potassium |
| Active Ingredient(s): | 200; 28.5 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: | 66685-1011 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065098 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20040813 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 66685-1011-0 |
| Package Description: | 50 mL in 1 BOTTLE (66685-1011-0) |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 66685-1011-0 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 50 mL in 1 BOTTLE (66685-1011-0) |
| Product NDC | 66685-1011 |
| 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 | 20040813 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 200; 28.5 |
| Strength Unit | mg/5mL; mg/5mL |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
