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Amoxicillin - 52959-613-02 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 52959-613
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: 52959-613
Labeler Name: H.J. Harkins Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065322
Marketing Category: ANDA
Start Marketing Date: 20060619

Package Information of Amoxicillin

Package NDC: 52959-613-02
Package Description: 100 mL in 1 BOTTLE (52959-613-02)

NDC Information of Amoxicillin

NDC Code 52959-613-02
Proprietary Name Amoxicillin
Package Description 100 mL in 1 BOTTLE (52959-613-02)
Product NDC 52959-613
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20060619
Marketing Category Name ANDA
Labeler Name H.J. Harkins Company, Inc.
Substance Name AMOXICILLIN
Strength Number 250
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Amoxicillin


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