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Amoxicillin - 0143-9888-80 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0143-9888
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: 0143-9888
Labeler Name: West-Ward Pharmaceutical Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065322
Marketing Category: ANDA
Start Marketing Date: 20060619

Package Information of Amoxicillin

Package NDC: 0143-9888-80
Package Description: 80 mL in 1 BOTTLE (0143-9888-80)

NDC Information of Amoxicillin

NDC Code 0143-9888-80
Proprietary Name Amoxicillin
Package Description 80 mL in 1 BOTTLE (0143-9888-80)
Product NDC 0143-9888
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 West-Ward Pharmaceutical Corp
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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