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AUGMENTIN ES-600 - 43598-003-51 - (amoxicillin and clavulanate potassium)

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Drug Information of AUGMENTIN ES-600

Product NDC: 43598-003
Proprietary Name: AUGMENTIN ES-600
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 600; 42.9    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 ES-600

Product NDC: 43598-003
Labeler Name: Dr Reddys Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050755
Marketing Category: NDA
Start Marketing Date: 20121031

Package Information of AUGMENTIN ES-600

Package NDC: 43598-003-51
Package Description: 75 mL in 1 BOTTLE (43598-003-51)

NDC Information of AUGMENTIN ES-600

NDC Code 43598-003-51
Proprietary Name AUGMENTIN ES-600
Package Description 75 mL in 1 BOTTLE (43598-003-51)
Product NDC 43598-003
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 20121031
Marketing Category Name NDA
Labeler Name Dr Reddys Laboratories Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 600; 42.9
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 ES-600


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