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Amoxicillin and Clavulanate Potassium - 68788-9961-2 - (amoxicillin and clavulanate potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 68788-9961
Proprietary Name: Amoxicillin and Clavulanate Potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 875; 125    mg/1; mg/1 & nbsp;   amoxicillin and clavulanate potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 68788-9961
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050564
Marketing Category: NDA
Start Marketing Date: 20120109

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 68788-9961-2
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (68788-9961-2)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 68788-9961-2
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (68788-9961-2)
Product NDC 68788-9961
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin and clavulanate potassium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120109
Marketing Category Name NDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 875; 125
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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