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Amoxicillin and Calvulanate Potassium
Amoxicillin and Calvulanate Potassium - 68084-235-01 - (Amoxicillin and Clavulanate Potassium)
Drug Information of Amoxicillin and Calvulanate Potassium
| Product NDC: | 68084-235 |
| Proprietary Name: | Amoxicillin and Calvulanate Potassium |
| Non Proprietary Name: | Amoxicillin and Clavulanate Potassium |
| Active Ingredient(s): | 500; 125 mg/1; mg/1 & nbsp; Amoxicillin and Clavulanate Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amoxicillin and Calvulanate Potassium
| Product NDC: | 68084-235 |
| Labeler Name: | American Health Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065109 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20091211 |
Package Information of Amoxicillin and Calvulanate Potassium
| Package NDC: | 68084-235-01 |
| Package Description: | 10 BLISTER PACK in 1 CARTON (68084-235-01) > 10 TABLET in 1 BLISTER PACK (68084-235-11) |
NDC Information of Amoxicillin and Calvulanate Potassium
| NDC Code | 68084-235-01 |
| Proprietary Name | Amoxicillin and Calvulanate Potassium |
| Package Description | 10 BLISTER PACK in 1 CARTON (68084-235-01) > 10 TABLET in 1 BLISTER PACK (68084-235-11) |
| Product NDC | 68084-235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091211 |
| Marketing Category Name | ANDA |
| Labeler Name | American Health Packaging |
| Substance Name | AMOXICILLIN; CLAVULANIC ACID |
| Strength Number | 500; 125 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
