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Amoxicillin and Clavulanate Potassium - 0781-1852-13 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 0781-1852
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: 0781-1852
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065063
Marketing Category: ANDA
Start Marketing Date: 20020314

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 0781-1852-13
Package Description: 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1852-13)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 0781-1852-13
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (0781-1852-13)
Product NDC 0781-1852
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 20020314
Marketing Category Name ANDA
Labeler Name Sandoz 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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