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Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate - 64720-136-11 - (Dextroamphetamine saccharate and amphetamine aspartate monohydrate and dextroamphetamine sulfate and amphetamine sulfate)

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Drug Information of Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate

Product NDC: 64720-136
Proprietary Name: Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate
Non Proprietary Name: Dextroamphetamine saccharate and amphetamine aspartate monohydrate and dextroamphetamine sulfate and amphetamine sulfate
Active Ingredient(s): 7.5; 7.5; 7.5; 7.5    mg/1; mg/1; mg/1; mg/1 & nbsp;   Dextroamphetamine saccharate and amphetamine aspartate monohydrate and dextroamphetamine sulfate and amphetamine sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate

Product NDC: 64720-136
Labeler Name: CorePharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040444
Marketing Category: ANDA
Start Marketing Date: 20070509

Package Information of Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate

Package NDC: 64720-136-11
Package Description: 1000 TABLET in 1 BOTTLE, PLASTIC (64720-136-11)

NDC Information of Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate

NDC Code 64720-136-11
Proprietary Name Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate
Package Description 1000 TABLET in 1 BOTTLE, PLASTIC (64720-136-11)
Product NDC 64720-136
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Dextroamphetamine saccharate and amphetamine aspartate monohydrate and dextroamphetamine sulfate and amphetamine sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070509
Marketing Category Name ANDA
Labeler Name CorePharma, LLC
Substance Name AMPHETAMINE ASPARTATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Strength Number 7.5; 7.5; 7.5; 7.5
Strength Unit mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE],Central Nervous System Stimulant [EPC],Central Nervous System Stimulation [PE]

Complete Information of Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate and amphetamine sulfate


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