Zenzedi - 24338-851-10 - (Dextroamphetamine Sulfate)

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Drug Information of Zenzedi

Product NDC: 24338-851
Proprietary Name: Zenzedi
Non Proprietary Name: Dextroamphetamine Sulfate
Active Ingredient(s): 5    mg/1 & nbsp;   Dextroamphetamine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Zenzedi

Product NDC: 24338-851
Labeler Name: Arbor Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090533
Marketing Category: ANDA
Start Marketing Date: 20130531

Package Information of Zenzedi

Package NDC: 24338-851-10
Package Description: 100 TABLET in 1 BOTTLE (24338-851-10)

NDC Information of Zenzedi

NDC Code 24338-851-10
Proprietary Name Zenzedi
Package Description 100 TABLET in 1 BOTTLE (24338-851-10)
Product NDC 24338-851
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130531
Marketing Category Name ANDA
Labeler Name Arbor Pharmaceuticals, Inc.
Substance Name DEXTROAMPHETAMINE SULFATE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Zenzedi


General Information