AUGMENTIN - 43598-018-30 - (amoxicillin and clavulanate potassium)

Alphabetical Index


Drug Information of AUGMENTIN

Product NDC: 43598-018
Proprietary Name: AUGMENTIN
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 250; 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 AUGMENTIN

Product NDC: 43598-018
Labeler Name: Dr. Reddy's Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050564
Marketing Category: NDA
Start Marketing Date: 19901022

Package Information of AUGMENTIN

Package NDC: 43598-018-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (43598-018-30)

NDC Information of AUGMENTIN

NDC Code 43598-018-30
Proprietary Name AUGMENTIN
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (43598-018-30)
Product NDC 43598-018
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 19901022
Marketing Category Name NDA
Labeler Name Dr. Reddy's Laboratories Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 250; 125
Strength Unit mg/1; mg/1
Pharmaceutical Classes beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA],Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of AUGMENTIN


General Information