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Amoxicillin - 54868-3105-2 - (amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 54868-3105
Proprietary Name: Amoxicillin
Non Proprietary Name: amoxicillin
Active Ingredient(s): 250    mg/1 & nbsp;   amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 54868-3105
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065021
Marketing Category: ANDA
Start Marketing Date: 20040601

Package Information of Amoxicillin

Package NDC: 54868-3105-2
Package Description: 20 TABLET, CHEWABLE in 1 BOTTLE (54868-3105-2)

NDC Information of Amoxicillin

NDC Code 54868-3105-2
Proprietary Name Amoxicillin
Package Description 20 TABLET, CHEWABLE in 1 BOTTLE (54868-3105-2)
Product NDC 54868-3105
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxicillin
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20040601
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXICILLIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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