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Amoxicillin/Clavulanate Potassium - 63629-1248-4 - (Amoxicillin/Clavulanate Potassium)

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Drug Information of Amoxicillin/Clavulanate Potassium

Product NDC: 63629-1248
Proprietary Name: Amoxicillin/Clavulanate Potassium
Non Proprietary Name: Amoxicillin/Clavulanate Potassium
Active Ingredient(s): 875; 125    mg/1; mg/1 & nbsp;   Amoxicillin/Clavulanate Potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin/Clavulanate Potassium

Product NDC: 63629-1248
Labeler Name: bryant ranch prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065093
Marketing Category: ANDA
Start Marketing Date: 20090612

Package Information of Amoxicillin/Clavulanate Potassium

Package NDC: 63629-1248-4
Package Description: 30 TABLET in 1 BOTTLE (63629-1248-4)

NDC Information of Amoxicillin/Clavulanate Potassium

NDC Code 63629-1248-4
Proprietary Name Amoxicillin/Clavulanate Potassium
Package Description 30 TABLET in 1 BOTTLE (63629-1248-4)
Product NDC 63629-1248
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin/Clavulanate Potassium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090612
Marketing Category Name ANDA
Labeler Name bryant ranch prepack
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 875; 125
Strength Unit mg/1; mg/1
Pharmaceutical Classes beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of Amoxicillin/Clavulanate Potassium


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