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Amoxicillin - 21695-294-00 - (Amoxicillin)

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Drug Information of Amoxicillin

Product NDC: 21695-294
Proprietary Name: Amoxicillin
Non Proprietary Name: Amoxicillin
Active Ingredient(s): 400    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: 21695-294
Labeler Name: Rebel Distributors Corp.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA065334
Marketing Category: ANDA
Start Marketing Date: 20061228

Package Information of Amoxicillin

Package NDC: 21695-294-00
Package Description: 100 mL in 1 BOTTLE (21695-294-00)

NDC Information of Amoxicillin

NDC Code 21695-294-00
Proprietary Name Amoxicillin
Package Description 100 mL in 1 BOTTLE (21695-294-00)
Product NDC 21695-294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Amoxicillin
Dosage Form Name POWDER, FOR SUSPENSION
Route Name ORAL
Start Marketing Date 20061228
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp.
Substance Name AMOXICILLIN
Strength Number 400
Strength Unit mg/5mL
Pharmaceutical Classes

Complete Information of Amoxicillin


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