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Amoxicillin - 0093-4150-79 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 0093-4150
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: 0093-4150
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061931
Marketing Category: ANDA
Start Marketing Date: 19900930

Package Information of Amoxicillin

Package NDC: 0093-4150-79
Package Description: 80 mL in 1 BOTTLE (0093-4150-79)

NDC Information of Amoxicillin

NDC Code 0093-4150-79
Proprietary Name Amoxicillin
Package Description 80 mL in 1 BOTTLE (0093-4150-79)
Product NDC 0093-4150
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 19900930
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
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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