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Amoxicillin and Clavulanate Potassium - 0781-1619-66 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0781-1619
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: 0781-1619
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065065
Marketing Category: ANDA
Start Marketing Date: 20020418

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 0781-1619-66
Package Description: 5 BLISTER PACK in 1 CARTON (0781-1619-66) > 4 TABLET, CHEWABLE in 1 BLISTER PACK

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 0781-1619-66
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 5 BLISTER PACK in 1 CARTON (0781-1619-66) > 4 TABLET, CHEWABLE in 1 BLISTER PACK
Product NDC 0781-1619
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin and Clavulanate Potassium
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20020418
Marketing Category Name ANDA
Labeler Name Sandoz 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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