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amoxicillin and clavulanate potassium - 43598-221-78 - (amoxicillin and clavulanate potassium)

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Drug Information of amoxicillin and clavulanate potassium

Product NDC: 43598-221
Proprietary Name: amoxicillin and clavulanate potassium
Non Proprietary Name: amoxicillin and clavulanate potassium
Active Ingredient(s): 875; 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 amoxicillin and clavulanate potassium

Product NDC: 43598-221
Labeler Name: Dr. Reddy's Laboratories Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA050720
Marketing Category: NDA
Start Marketing Date: 19961002

Package Information of amoxicillin and clavulanate potassium

Package NDC: 43598-221-78
Package Description: 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (43598-221-78)

NDC Information of amoxicillin and clavulanate potassium

NDC Code 43598-221-78
Proprietary Name amoxicillin and clavulanate potassium
Package Description 100 TABLET, FILM COATED in 1 BOX, UNIT-DOSE (43598-221-78)
Product NDC 43598-221
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 19961002
Marketing Category Name NDA
Labeler Name Dr. Reddy's Laboratories Inc
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 875; 125
Strength Unit mg/1; mg/1
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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