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AMOXICILLIN - 16590-647-90 - (AMOXICILLIN)

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Drug Information of AMOXICILLIN

Product NDC: 16590-647
Proprietary Name: AMOXICILLIN
Non Proprietary Name: AMOXICILLIN
Active Ingredient(s): 125    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: 16590-647
Labeler Name: STAT RX USA LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA064013
Marketing Category: ANDA
Start Marketing Date: 20100128

Package Information of AMOXICILLIN

Package NDC: 16590-647-90
Package Description: 90 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16590-647-90)

NDC Information of AMOXICILLIN

NDC Code 16590-647-90
Proprietary Name AMOXICILLIN
Package Description 90 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (16590-647-90)
Product NDC 16590-647
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name AMOXICILLIN
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20100128
Marketing Category Name ANDA
Labeler Name STAT RX USA LLC
Substance Name AMOXICILLIN
Strength Number 125
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of AMOXICILLIN


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