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Amoxicillin and Clavulanate Potassium - 67296-0716-1 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 67296-0716
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: 67296-0716
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065109
Marketing Category: ANDA
Start Marketing Date: 20080201

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 67296-0716-1
Package Description: 14 TABLET, FILM COATED in 1 BOTTLE (67296-0716-1)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 67296-0716-1
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 14 TABLET, FILM COATED in 1 BOTTLE (67296-0716-1)
Product NDC 67296-0716
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 20080201
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
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 and Clavulanate Potassium


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