AUGMENTIN - 43598-020-28 - (amoxicillin and clavulanate potassium)

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Drug Information of AUGMENTIN

Product NDC: 43598-020
Proprietary Name: AUGMENTIN
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 562.5; 437.5; 62.5    mg/1; mg/1; mg/1 & nbsp;   amoxicillin and clavulanate potassium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of AUGMENTIN

Product NDC: 43598-020
Labeler Name: Dr Reddys Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050785
Marketing Category: NDA
Start Marketing Date: 20030911

Package Information of AUGMENTIN

Package NDC: 43598-020-28
Package Description: 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43598-020-28)

NDC Information of AUGMENTIN

NDC Code 43598-020-28
Proprietary Name AUGMENTIN
Package Description 28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (43598-020-28)
Product NDC 43598-020
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin and clavulanate potassium
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20030911
Marketing Category Name NDA
Labeler Name Dr Reddys Laboratories Inc
Substance Name AMOXICILLIN; AMOXICILLIN SODIUM; CLAVULANATE POTASSIUM
Strength Number 562.5; 437.5; 62.5
Strength Unit mg/1; mg/1; mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of AUGMENTIN


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