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Amoxicillin - 67296-0023-1 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 67296-0023
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 250    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 67296-0023
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061926
Marketing Category: ANDA
Start Marketing Date: 20100128

Package Information of Amoxicillin

Package NDC: 67296-0023-1
Package Description: 30 CAPSULE in 1 BOTTLE (67296-0023-1)

NDC Information of Amoxicillin

NDC Code 67296-0023-1
Proprietary Name Amoxicillin
Package Description 30 CAPSULE in 1 BOTTLE (67296-0023-1)
Product NDC 67296-0023
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100128
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
Substance Name AMOXICILLIN
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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