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Amoxicillin - 67296-0628-1 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 67296-0628
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: 67296-0628
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065255
Marketing Category: ANDA
Start Marketing Date: 20060329

Package Information of Amoxicillin

Package NDC: 67296-0628-1
Package Description: 20 TABLET, COATED in 1 BOTTLE (67296-0628-1)

NDC Information of Amoxicillin

NDC Code 67296-0628-1
Proprietary Name Amoxicillin
Package Description 20 TABLET, COATED in 1 BOTTLE (67296-0628-1)
Product NDC 67296-0628
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 RedPharm Drug 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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