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Amoxicillin - 65862-065-05 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 65862-065
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 200    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 65862-065
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065324
Marketing Category: ANDA
Start Marketing Date: 20070117

Package Information of Amoxicillin

Package NDC: 65862-065-05
Package Description: 500 TABLET, FOR SUSPENSION in 1 BOTTLE (65862-065-05)

NDC Information of Amoxicillin

NDC Code 65862-065-05
Proprietary Name Amoxicillin
Package Description 500 TABLET, FOR SUSPENSION in 1 BOTTLE (65862-065-05)
Product NDC 65862-065
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070117
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name AMOXICILLIN
Strength Number 200
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Amoxicillin


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