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Amoxicillin and Clavulanate Potassium - 0093-2270-34 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0093-2270
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: Amoxicillin and Clavulanate Potassium
Active Ingredient(s): 200; 28.5    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: 0093-2270
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065205
Marketing Category: ANDA
Start Marketing Date: 20050322

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 0093-2270-34
Package Description: 20 TABLET, CHEWABLE in 1 BOTTLE (0093-2270-34)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 0093-2270-34
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 20 TABLET, CHEWABLE in 1 BOTTLE (0093-2270-34)
Product NDC 0093-2270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin and Clavulanate Potassium
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20050322
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 200; 28.5
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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