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Amoxicillin - 0781-5060-20 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0781-5060
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 500    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: 0781-5060
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065228
Marketing Category: ANDA
Start Marketing Date: 20050713

Package Information of Amoxicillin

Package NDC: 0781-5060-20
Package Description: 20 TABLET, FILM COATED in 1 BOTTLE (0781-5060-20)

NDC Information of Amoxicillin

NDC Code 0781-5060-20
Proprietary Name Amoxicillin
Package Description 20 TABLET, FILM COATED in 1 BOTTLE (0781-5060-20)
Product NDC 0781-5060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20050713
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMOXICILLIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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