Home
>
National Drug Code (NDC)
>
Amoxicillin and Clavulanate Potassium
Amoxicillin and Clavulanate Potassium - 21695-214-20 - (Amoxicillin and Clavulanate Potassium)
Drug Information of Amoxicillin and Clavulanate Potassium
| Product NDC: | 21695-214 |
| 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: | 21695-214 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065101 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20021030 |
Package Information of Amoxicillin and Clavulanate Potassium
| Package NDC: | 21695-214-20 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE (21695-214-20) |
NDC Information of Amoxicillin and Clavulanate Potassium
| NDC Code | 21695-214-20 |
| Proprietary Name | Amoxicillin and Clavulanate Potassium |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (21695-214-20) |
| Product NDC | 21695-214 |
| 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 | 20021030 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 500; 125 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
