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Amoxicillin - 67296-0616-6 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 67296-0616
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 500    mg/1 & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 67296-0616
Labeler Name: RedPharm Drug Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065271
Marketing Category: ANDA
Start Marketing Date: 20050911

Package Information of Amoxicillin

Package NDC: 67296-0616-6
Package Description: 21 CAPSULE in 1 BOTTLE (67296-0616-6)

NDC Information of Amoxicillin

NDC Code 67296-0616-6
Proprietary Name Amoxicillin
Package Description 21 CAPSULE in 1 BOTTLE (67296-0616-6)
Product NDC 67296-0616
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20050911
Marketing Category Name ANDA
Labeler Name RedPharm Drug Inc.
Substance Name AMOXICILLIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes Penicillin-class Antibacterial [EPC],Penicillins [Chemical/Ingredient]

Complete Information of Amoxicillin


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