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Amoxicillin - 54868-4543-3 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 54868-4543
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 875    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 54868-4543
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065228
Marketing Category: ANDA
Start Marketing Date: 20020312

Package Information of Amoxicillin

Package NDC: 54868-4543-3
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (54868-4543-3)

NDC Information of Amoxicillin

NDC Code 54868-4543-3
Proprietary Name Amoxicillin
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (54868-4543-3)
Product NDC 54868-4543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20020312
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXICILLIN
Strength Number 875
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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