"0555-0762-02" National Drug Code (NDC)

NDC Code	0555-0762-02
Package Description	100 TABLET in 1 BOTTLE (0555-0762-02)
Product NDC	0555-0762
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Adderall
Non-Proprietary Name	Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate, And Amphetamine Sulfate
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20080811
End Marketing Date	20150831
Marketing Category Name	ANDA
Application Number	ANDA040422
Manufacturer	Barr Laboratories Inc.
Substance Name	AMPHETAMINE ASPARTATE MONOHYDRATE; AMPHETAMINE SULFATE; DEXTROAMPHETAMINE SACCHARATE; DEXTROAMPHETAMINE SULFATE
Strength	1.25; 1.25; 1.25; 1.25
Strength Unit	mg/1; mg/1; mg/1; mg/1
Pharmacy 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]
DEA Schedule	CII