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Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 66685-1002-0 - (amoxicillin and clavulanate potassium)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 66685-1002 |
| Proprietary Name: | Amoxicillin and Clavulanate 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, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 66685-1002 |
| Labeler Name: | Sandoz Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065117 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20021127 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 66685-1002-0 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE (66685-1002-0) |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 66685-1002-0 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (66685-1002-0) |
| Product NDC | 66685-1002 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amoxicillin and clavulanate potassium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20021127 |
| Marketing Category Name | ANDA |
| Labeler Name | Sandoz Inc |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 500; 125 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
