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Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 53808-0759-1 - (AMOXICILLIN AND CLAVULANATE POTASSIUM)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 53808-0759 |
| Proprietary Name: | Amoxicillin and Clavulanate Potassium |
| Non Proprietary Name: | AMOXICILLIN AND CLAVULANATE POTASSIUM |
| Active Ingredient(s): | 250; 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: | 53808-0759 |
| Labeler Name: | State of Florida DOH Central Pharmacy |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065189 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090701 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 53808-0759-1 |
| Package Description: | 30 DOSE PACK in 1 CARTON (53808-0759-1) > 1 TABLET, FILM COATED in 1 DOSE PACK |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 53808-0759-1 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 30 DOSE PACK in 1 CARTON (53808-0759-1) > 1 TABLET, FILM COATED in 1 DOSE PACK |
| Product NDC | 53808-0759 |
| 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 | 20090701 |
| Marketing Category Name | ANDA |
| Labeler Name | State of Florida DOH Central Pharmacy |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 250; 125 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
