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Amoxicillin - 55289-707-20 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 55289-707
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 875    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): TABLET, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 55289-707
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065255
Marketing Category: ANDA
Start Marketing Date: 20060329

Package Information of Amoxicillin

Package NDC: 55289-707-20
Package Description: 20 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-707-20)

NDC Information of Amoxicillin

NDC Code 55289-707-20
Proprietary Name Amoxicillin
Package Description 20 TABLET, COATED in 1 BOTTLE, PLASTIC (55289-707-20)
Product NDC 55289-707
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20060329
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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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