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Amoxicillin - 49999-015-14 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 49999-015
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: 49999-015
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065291
Marketing Category: ANDA
Start Marketing Date: 20111215

Package Information of Amoxicillin

Package NDC: 49999-015-14
Package Description: 14 CAPSULE in 1 BOTTLE (49999-015-14)

NDC Information of Amoxicillin

NDC Code 49999-015-14
Proprietary Name Amoxicillin
Package Description 14 CAPSULE in 1 BOTTLE (49999-015-14)
Product NDC 49999-015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20111215
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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