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Amoxicillin - 42291-120-50 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 42291-120
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: 42291-120
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA062058
Marketing Category: ANDA
Start Marketing Date: 20110809

Package Information of Amoxicillin

Package NDC: 42291-120-50
Package Description: 500 CAPSULE in 1 BOTTLE (42291-120-50)

NDC Information of Amoxicillin

NDC Code 42291-120-50
Proprietary Name Amoxicillin
Package Description 500 CAPSULE in 1 BOTTLE (42291-120-50)
Product NDC 42291-120
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110809
Marketing Category Name ANDA
Labeler Name AvKARE, 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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