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Dextroamphetamine Sulfate - 54868-5479-1 - (Dextroamphetamine Sulfate)

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Drug Information of Dextroamphetamine Sulfate

Product NDC: 54868-5479
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: 54868-5479
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076137
Marketing Category: ANDA
Start Marketing Date: 20051130

Package Information of Dextroamphetamine Sulfate

Package NDC: 54868-5479-1
Package Description: 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5479-1)

NDC Information of Dextroamphetamine Sulfate

NDC Code 54868-5479-1
Proprietary Name Dextroamphetamine Sulfate
Package Description 20 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-5479-1)
Product NDC 54868-5479
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine Sulfate
Dosage Form Name CAPSULE, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20051130
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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