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dextroamphetamine sulfate - 58177-311-09 - (dextroamphetamine sulfate)

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Drug Information of dextroamphetamine sulfate

Product NDC: 58177-311
Proprietary Name: dextroamphetamine sulfate
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 dextroamphetamine sulfate

Product NDC: 58177-311
Labeler Name: Ethex Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040365
Marketing Category: ANDA
Start Marketing Date: 20091101

Package Information of dextroamphetamine sulfate

Package NDC: 58177-311-09
Package Description: 1000 TABLET in 1 BOTTLE (58177-311-09)

NDC Information of dextroamphetamine sulfate

NDC Code 58177-311-09
Proprietary Name dextroamphetamine sulfate
Package Description 1000 TABLET in 1 BOTTLE (58177-311-09)
Product NDC 58177-311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name dextroamphetamine sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091101
Marketing Category Name ANDA
Labeler Name Ethex Corporation
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 dextroamphetamine sulfate


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