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Amoxicillin and Clavulanate Potassium - 66685-1011-0 - (amoxicillin and clavulanate potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 66685-1011
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 200; 28.5    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: 66685-1011
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065098
Marketing Category: ANDA
Start Marketing Date: 20040813

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 66685-1011-0
Package Description: 50 mL in 1 BOTTLE (66685-1011-0)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 66685-1011-0
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 50 mL in 1 BOTTLE (66685-1011-0)
Product NDC 66685-1011
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 20040813
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 200; 28.5
Strength Unit mg/5mL; mg/5mL
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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