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Amoxicillin - 50436-7218-3 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 50436-7218
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: 50436-7218
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065291
Marketing Category: ANDA
Start Marketing Date: 20070301

Package Information of Amoxicillin

Package NDC: 50436-7218-3
Package Description: 6 CAPSULE in 1 BOTTLE (50436-7218-3)

NDC Information of Amoxicillin

NDC Code 50436-7218-3
Proprietary Name Amoxicillin
Package Description 6 CAPSULE in 1 BOTTLE (50436-7218-3)
Product NDC 50436-7218
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070301
Marketing Category Name ANDA
Labeler Name Unit Dose Services
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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