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Amoxicillin and Clavulanate Potassium - 60505-2540-2 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 60505-2540
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
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 60505-2540
Labeler Name: Apotex Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065333
Marketing Category: ANDA
Start Marketing Date: 20090706

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 60505-2540-2
Package Description: 20 TABLET in 1 BOTTLE (60505-2540-2)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 60505-2540-2
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 20 TABLET in 1 BOTTLE (60505-2540-2)
Product NDC 60505-2540
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin and Clavulanate Potassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090706
Marketing Category Name ANDA
Labeler Name Apotex Corp.
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 500; 125
Strength Unit mg/1; mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of Amoxicillin and Clavulanate Potassium


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