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Dextroamphetamine Sulfate - 52536-510-01 - (Dextroamphetamine Sulfate)

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Drug Information of Dextroamphetamine Sulfate

Product NDC: 52536-510
Proprietary Name: Dextroamphetamine Sulfate
Non Proprietary Name: Dextroamphetamine Sulfate
Active Ingredient(s): 10    mg/1 & nbsp;   Dextroamphetamine Sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dextroamphetamine Sulfate

Product NDC: 52536-510
Labeler Name: Wilshire Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090533
Marketing Category: ANDA
Start Marketing Date: 20120720

Package Information of Dextroamphetamine Sulfate

Package NDC: 52536-510-01
Package Description: 100 TABLET in 1 BOTTLE (52536-510-01)

NDC Information of Dextroamphetamine Sulfate

NDC Code 52536-510-01
Proprietary Name Dextroamphetamine Sulfate
Package Description 100 TABLET in 1 BOTTLE (52536-510-01)
Product NDC 52536-510
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine Sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120720
Marketing Category Name ANDA
Labeler Name Wilshire Pharmaceuticals, Inc.
Substance Name DEXTROAMPHETAMINE SULFATE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Dextroamphetamine Sulfate


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