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Amoxicillin - 68788-9710-3 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 68788-9710
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: 68788-9710
Labeler Name: Preferred Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065271
Marketing Category: ANDA
Start Marketing Date: 20130130

Package Information of Amoxicillin

Package NDC: 68788-9710-3
Package Description: 30 CAPSULE in 1 BOTTLE (68788-9710-3)

NDC Information of Amoxicillin

NDC Code 68788-9710-3
Proprietary Name Amoxicillin
Package Description 30 CAPSULE in 1 BOTTLE (68788-9710-3)
Product NDC 68788-9710
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130130
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, 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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