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Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 0781-1943-82 - (Amoxicillin and Clavulanate Potassium)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 0781-1943 |
| Proprietary Name: | Amoxicillin and Clavulanate Potassium |
| Non Proprietary Name: | Amoxicillin and Clavulanate Potassium |
| Active Ingredient(s): | 562.5; 437.5; 62.5 mg/1; mg/1; mg/1 & nbsp; Amoxicillin and Clavulanate Potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, MULTILAYER, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 0781-1943 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA090227 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100421 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 0781-1943-82 |
| Package Description: | 28 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-82) |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 0781-1943-82 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 28 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-82) |
| Product NDC | 0781-1943 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Dosage Form Name | TABLET, MULTILAYER, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100421 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM |
| Strength Number | 562.5; 437.5; 62.5 |
| Strength Unit | mg/1; mg/1; mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
