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Amoxicillin and Clavulanate Potassium - 0781-1943-39 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0781-1943
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: Amoxicillin and Clavulanate Potassium
Active Ingredient(s): 562.5; 437.5; 62.5    mg/1; mg/1; mg/1 & nbsp;   Amoxicillin and Clavulanate Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, MULTILAYER, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0781-1943
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090227
Marketing Category: ANDA
Start Marketing Date: 20100421

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 0781-1943-39
Package Description: 40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-39)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 0781-1943-39
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 40 TABLET, MULTILAYER, EXTENDED RELEASE in 1 BOTTLE (0781-1943-39)
Product NDC 0781-1943
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin and Clavulanate Potassium
Dosage Form Name TABLET, MULTILAYER, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20100421
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM
Strength Number 562.5; 437.5; 62.5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],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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