AUGMENTIN - 43598-004-53 - (amoxicillin and clavulanate potassium)

Alphabetical Index


Drug Information of AUGMENTIN

Product NDC: 43598-004
Proprietary Name: AUGMENTIN
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 250; 62.5    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 AUGMENTIN

Product NDC: 43598-004
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 AUGMENTIN

Package NDC: 43598-004-53
Package Description: 150 mL in 1 BOTTLE (43598-004-53)

NDC Information of AUGMENTIN

NDC Code 43598-004-53
Proprietary Name AUGMENTIN
Package Description 150 mL in 1 BOTTLE (43598-004-53)
Product NDC 43598-004
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 250; 62.5
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 AUGMENTIN


General Information