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AugmentinXR - 54868-4735-0 - (amoxicillin and clavulanate potassium)

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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]

Complete Information of AugmentinXR


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