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Amoxicillin - 65862-015-20 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 65862-015
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 875    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 65862-015
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065256
Marketing Category: ANDA
Start Marketing Date: 20051109

Package Information of Amoxicillin

Package NDC: 65862-015-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)

NDC Information of Amoxicillin

NDC Code 65862-015-20
Proprietary Name Amoxicillin
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (65862-015-20)
Product NDC 65862-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20051109
Marketing Category Name ANDA
Labeler Name Aurobindo Pharma Limited
Substance Name AMOXICILLIN
Strength Number 875
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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