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Amoxicillin and Clavulanate Potassium - 60432-065-75 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 60432-065
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: Amoxicillin and Clavulanate Potassium
Active Ingredient(s): 250; 62.5    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: 60432-065
Labeler Name: Morton Grove Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065431
Marketing Category: ANDA
Start Marketing Date: 20090701

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 60432-065-75
Package Description: 75 mL in 1 BOTTLE, PLASTIC (60432-065-75)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 60432-065-75
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 75 mL in 1 BOTTLE, PLASTIC (60432-065-75)
Product NDC 60432-065
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 20090701
Marketing Category Name ANDA
Labeler Name Morton Grove Pharmaceuticals, Inc.
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 250; 62.5
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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