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Amoxicillin - 54868-3109-6 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 54868-3109
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 500    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 54868-3109
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064076
Marketing Category: ANDA
Start Marketing Date: 19940930

Package Information of Amoxicillin

Package NDC: 54868-3109-6
Package Description: 9 CAPSULE in 1 BOTTLE (54868-3109-6)

NDC Information of Amoxicillin

NDC Code 54868-3109-6
Proprietary Name Amoxicillin
Package Description 9 CAPSULE in 1 BOTTLE (54868-3109-6)
Product NDC 54868-3109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19940930
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXICILLIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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