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Amoxicillin - 0781-6157-57 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0781-6157
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 400    mg/5mL & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 0781-6157
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065378
Marketing Category: ANDA
Start Marketing Date: 20070326

Package Information of Amoxicillin

Package NDC: 0781-6157-57
Package Description: 75 mL in 1 BOTTLE (0781-6157-57)

NDC Information of Amoxicillin

NDC Code 0781-6157-57
Proprietary Name Amoxicillin
Package Description 75 mL in 1 BOTTLE (0781-6157-57)
Product NDC 0781-6157
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20070326
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name AMOXICILLIN
Strength Number 400
Strength Unit mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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