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Amoxicillin and Clavulanate Potassium - 21695-401-20 - (Amoxicillin and Clavulanate Potassium)

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Drug Information of Amoxicillin and Clavulanate Potassium

Product NDC: 21695-401
Proprietary Name: Amoxicillin and Clavulanate Potassium
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): SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin and Clavulanate Potassium

Product NDC: 21695-401
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065358
Marketing Category: ANDA
Start Marketing Date: 20070813

Package Information of Amoxicillin and Clavulanate Potassium

Package NDC: 21695-401-20
Package Description: 200 mL in 1 BOTTLE, DISPENSING (21695-401-20)

NDC Information of Amoxicillin and Clavulanate Potassium

NDC Code 21695-401-20
Proprietary Name Amoxicillin and Clavulanate Potassium
Package Description 200 mL in 1 BOTTLE, DISPENSING (21695-401-20)
Product NDC 21695-401
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin and Clavulanate Potassium
Dosage Form Name SUSPENSION
Route Name ORAL
Start Marketing Date 20070813
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name AMOXICILLIN; CLAVULANATE POTASSIUM
Strength Number 600; 42.9
Strength Unit mg/5mL; mg/5mL
Pharmaceutical Classes beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]

Complete Information of Amoxicillin and Clavulanate Potassium


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