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Amoxicillin and Clavulanate Potassium - 54868-0286-0 - (amoxicillin and clavulanate potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 54868-0286
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 400; 57    mg/1; mg/1 & nbsp;   amoxicillin and clavulanate potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 54868-0286
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065161
Marketing Category: ANDA
Start Marketing Date: 20070813

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 54868-0286-0
Package Description: 20 TABLET, CHEWABLE in 1 BOTTLE (54868-0286-0)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 54868-0286-0
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 20 TABLET, CHEWABLE in 1 BOTTLE (54868-0286-0)
Product NDC 54868-0286
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin and clavulanate potassium
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20070813
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 400; 57
Strength Unit mg/1; mg/1
Pharmaceutical Classes beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of Amoxicillin and Clavulanate Potassium


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