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Amoxicillin/Clavulanate Potassium
Amoxicillin/Clavulanate Potassium - 63629-1248-4 - (Amoxicillin/Clavulanate Potassium)
Drug Information of Amoxicillin/Clavulanate Potassium
| Product NDC: | 63629-1248 |
| Proprietary Name: | Amoxicillin/Clavulanate Potassium |
| Non Proprietary Name: | Amoxicillin/Clavulanate Potassium |
| Active Ingredient(s): | 875; 125 mg/1; mg/1 & nbsp; Amoxicillin/Clavulanate Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amoxicillin/Clavulanate Potassium
| Product NDC: | 63629-1248 |
| Labeler Name: | bryant ranch prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065093 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090612 |
Package Information of Amoxicillin/Clavulanate Potassium
| Package NDC: | 63629-1248-4 |
| Package Description: | 30 TABLET in 1 BOTTLE (63629-1248-4) |
NDC Information of Amoxicillin/Clavulanate Potassium
| NDC Code | 63629-1248-4 |
| Proprietary Name | Amoxicillin/Clavulanate Potassium |
| Package Description | 30 TABLET in 1 BOTTLE (63629-1248-4) |
| Product NDC | 63629-1248 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amoxicillin/Clavulanate Potassium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20090612 |
| Marketing Category Name | ANDA |
| Labeler Name | bryant ranch prepack |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 875; 125 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
