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AugmentinXR
AugmentinXR - 54868-4735-0 - (amoxicillin and clavulanate potassium)
Drug Information of AugmentinXR
| Product NDC: | 54868-4735 |
| Proprietary Name: | AugmentinXR |
| Non Proprietary Name: | amoxicillin and clavulanate potassium |
| Active Ingredient(s): | 1000; 62.5 mg/1; mg/1 & nbsp; amoxicillin and clavulanate potassium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of AugmentinXR
| Product NDC: | 54868-4735 |
| Labeler Name: | Physicians Total Care, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050785 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20030130 |
Package Information of AugmentinXR
| Package NDC: | 54868-4735-0 |
| Package Description: | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4735-0) |
NDC Information of AugmentinXR
| NDC Code | 54868-4735-0 |
| Proprietary Name | AugmentinXR |
| Package Description | 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4735-0) |
| Product NDC | 54868-4735 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | amoxicillin and clavulanate potassium |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20030130 |
| Marketing Category Name | NDA |
| Labeler Name | Physicians Total Care, Inc. |
| Substance Name | AMOXICILLIN; CLAVULANATE POTASSIUM |
| Strength Number | 1000; 62.5 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA] |
