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Amoxicillin and Clavulanate Potassium - 54868-5175-0 - (amoxicillin and clavulanate potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 54868-5175
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 400; 57    mg/5mL; mg/5mL & nbsp;   amoxicillin and clavulanate potassium
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 54868-5175
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065066
Marketing Category: ANDA
Start Marketing Date: 20050316

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 54868-5175-0
Package Description: 100 mL in 1 BOTTLE (54868-5175-0)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 54868-5175-0
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 100 mL in 1 BOTTLE (54868-5175-0)
Product NDC 54868-5175
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin and clavulanate potassium
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20050316
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 400; 57
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of Amoxicillin and Clavulanate Potassium


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