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Amoxicillin - 21695-315-30 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 21695-315
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: 21695-315
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065271
Marketing Category: ANDA
Start Marketing Date: 20050911

Package Information of Amoxicillin

Package NDC: 21695-315-30
Package Description: 30 CAPSULE in 1 BOTTLE (21695-315-30)

NDC Information of Amoxicillin

NDC Code 21695-315-30
Proprietary Name Amoxicillin
Package Description 30 CAPSULE in 1 BOTTLE (21695-315-30)
Product NDC 21695-315
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 Rebel Distributors Corp.
Substance Name AMOXICILLIN
Strength Number 500
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Amoxicillin


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