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Dextroamphetamine - 27808-085-01 - (Dextroamphetamine)

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Drug Information of Dextroamphetamine

Product NDC: 27808-085
Proprietary Name: Dextroamphetamine
Non Proprietary Name: Dextroamphetamine
Active Ingredient(s): 5    mg/5mL & nbsp;   Dextroamphetamine
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Dextroamphetamine

Product NDC: 27808-085
Labeler Name: Tris Pharma Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA203644
Marketing Category: ANDA
Start Marketing Date: 20130531

Package Information of Dextroamphetamine

Package NDC: 27808-085-01
Package Description: 473 mL in 1 BOTTLE, PLASTIC (27808-085-01)

NDC Information of Dextroamphetamine

NDC Code 27808-085-01
Proprietary Name Dextroamphetamine
Package Description 473 mL in 1 BOTTLE, PLASTIC (27808-085-01)
Product NDC 27808-085
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 20130531
Marketing Category Name ANDA
Labeler Name Tris Pharma Inc
Substance Name DEXTROAMPHETAMINE SULFATE
Strength Number 5
Strength Unit mg/5mL
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Dextroamphetamine


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