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Amoxicillin - 59762-1020-1 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 59762-1020
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: 59762-1020
Labeler Name: Greenstone LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065271
Marketing Category: ANDA
Start Marketing Date: 20050911

Package Information of Amoxicillin

Package NDC: 59762-1020-1
Package Description: 100 CAPSULE in 1 BOTTLE (59762-1020-1)

NDC Information of Amoxicillin

NDC Code 59762-1020-1
Proprietary Name Amoxicillin
Package Description 100 CAPSULE in 1 BOTTLE (59762-1020-1)
Product NDC 59762-1020
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 Greenstone LLC
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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