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Amoxicillin - 68788-9948-1 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 68788-9948
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 250    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: 68788-9948
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065387
Marketing Category: ANDA
Start Marketing Date: 20120112

Package Information of Amoxicillin

Package NDC: 68788-9948-1
Package Description: 150 mL in 1 BOTTLE (68788-9948-1)

NDC Information of Amoxicillin

NDC Code 68788-9948-1
Proprietary Name Amoxicillin
Package Description 150 mL in 1 BOTTLE (68788-9948-1)
Product NDC 68788-9948
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20120112
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name AMOXICILLIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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