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Amoxicillin and Clavulanate Potassium - 0093-8675-74 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0093-8675
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: Amoxicillin and Clavulanate Potassium
Active Ingredient(s): 600; 42.9    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: 0093-8675
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065162
Marketing Category: ANDA
Start Marketing Date: 20040923

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 0093-8675-74
Package Description: 200 mL in 1 BOTTLE (0093-8675-74)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 0093-8675-74
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 200 mL in 1 BOTTLE (0093-8675-74)
Product NDC 0093-8675
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 20040923
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 600; 42.9
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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