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Amoxicillin - 21695-384-15 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 21695-384
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 125    mg/5mL & nbsp;   Amoxicillin
Administration Route(s): ORAL
Dosage Form(s): POWDER, FOR SUSPENSION
Coding System: National Drug Codes(NDC)

Labeler Information of Amoxicillin

Product NDC: 21695-384
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA061931
Marketing Category: ANDA
Start Marketing Date: 20100201

Package Information of Amoxicillin

Package NDC: 21695-384-15
Package Description: 150 mL in 1 BOTTLE (21695-384-15)

NDC Information of Amoxicillin

NDC Code 21695-384-15
Proprietary Name Amoxicillin
Package Description 150 mL in 1 BOTTLE (21695-384-15)
Product NDC 21695-384
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20100201
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name AMOXICILLIN
Strength Number 125
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Amoxicillin


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