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Dextroamphetamine Sulfate - 64720-328-09 - (Dextroamphetamine Sulfate)

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Drug Information of Dextroamphetamine Sulfate

Product NDC: 64720-328
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): CAPSULE, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Dextroamphetamine Sulfate

Product NDC: 64720-328
Labeler Name: Corepharma LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA017078
Marketing Category: NDA
Start Marketing Date: 20110901

Package Information of Dextroamphetamine Sulfate

Package NDC: 64720-328-09
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64720-328-09)

NDC Information of Dextroamphetamine Sulfate

NDC Code 64720-328-09
Proprietary Name Dextroamphetamine Sulfate
Package Description 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (64720-328-09)
Product NDC 64720-328
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine Sulfate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110901
Marketing Category Name NDA
Labeler Name Corepharma LLC.
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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