NDC Code | 68084-909-32 |
Package Description | 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-909-32) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-909-33) |
Product NDC | 68084-909 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate |
Non-Proprietary Name | Dextroamphetamine Saccharate, Amphetamine Aspartate, Dextroamphetamine Sulfate And Amphetamine Sulfate |
Dosage Form | CAPSULE, EXTENDED RELEASE |
Usage | ORAL |
Start Marketing Date | 20141215 |
End Marketing Date | 20171231 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA021303 |
Manufacturer | American Health Packaging |
Substance Name | DEXTROAMPHETAMINE SACCHARATE; AMPHETAMINE ASPARTATE MONOHYDRATE; DEXTROAMPHETAMINE SULFATE; AMPHETAMINE SULFATE |
Strength | 6.25; 6.25; 6.25; 6.25 |
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 |