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Amoxicillin - 54569-2928-0 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 54569-2928
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 125    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: 54569-2928
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065322
Marketing Category: ANDA
Start Marketing Date: 20060619

Package Information of Amoxicillin

Package NDC: 54569-2928-0
Package Description: 100 mL in 1 BOTTLE (54569-2928-0)

NDC Information of Amoxicillin

NDC Code 54569-2928-0
Proprietary Name Amoxicillin
Package Description 100 mL in 1 BOTTLE (54569-2928-0)
Product NDC 54569-2928
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20060619
Marketing Category Name ANDA
Labeler Name A-S Medication Solutions LLC
Substance Name AMOXICILLIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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