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AMOXICILLIN AND CLAVULANATE POTASSIUM
AMOXICILLIN AND CLAVULANATE POTASSIUM - 16590-019-20 - (AMOXICILLIN AND CLAVULANATE POTASSIUM)
Drug Information of AMOXICILLIN AND CLAVULANATE POTASSIUM
| Product NDC: | 16590-019 |
| 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: | 16590-019 |
| Labeler Name: | STAT RX USA LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065101 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20110125 |
Package Information of AMOXICILLIN AND CLAVULANATE POTASSIUM
| Package NDC: | 16590-019-20 |
| Package Description: | 20 TABLET, FILM COATED in 1 BOTTLE (16590-019-20) |
NDC Information of AMOXICILLIN AND CLAVULANATE POTASSIUM
| NDC Code | 16590-019-20 |
| Proprietary Name | AMOXICILLIN AND CLAVULANATE POTASSIUM |
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (16590-019-20) |
| Product NDC | 16590-019 |
| 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 | 20110125 |
| Marketing Category Name | ANDA |
| Labeler Name | STAT RX USA LLC |
| 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] |
