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amoxicillin and clavulanate potassium - 43598-213-50 - (amoxicillin and clavulanate potassium)

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Drug Information of amoxicillin and clavulanate potassium

Product NDC: 43598-213
Proprietary Name: amoxicillin and clavulanate potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 200; 28.5    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: 43598-213
Labeler Name: Dr. Reddy's Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050575
Marketing Category: NDA
Start Marketing Date: 19901022

Package Information of amoxicillin and clavulanate potassium

Package NDC: 43598-213-50
Package Description: 50 mL in 1 BOTTLE (43598-213-50)

NDC Information of amoxicillin and clavulanate potassium

NDC Code 43598-213-50
Proprietary Name amoxicillin and clavulanate potassium
Package Description 50 mL in 1 BOTTLE (43598-213-50)
Product NDC 43598-213
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 19901022
Marketing Category Name NDA
Labeler Name Dr. Reddy's Laboratories Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 200; 28.5
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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