Details for New Drug Application (NDA): 211546
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The generic ingredient in DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE is amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate. There are fifty-five drug master file entries for this compound. Twenty-eight suppliers are listed for this compound. Additional details are available on the amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate profile page.
Summary for 211546
Pharmacology for NDA: 211546
Physiological Effect | Central Nervous System Stimulation |
Suppliers and Packaging for NDA: 211546
Tradename | Generic Name | Dosage | NDA | Application Type | Supplier | National Drug Code | Package Code | Package |
---|---|---|---|---|---|---|---|---|
DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE | amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate | CAPSULE, EXTENDED RELEASE;ORAL | 211546 | ANDA | SpecGx LLC | 0406-0803 | 0406-0803-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0406-0803-01) |
DEXTROAMP SACCHARATE, AMP ASPARTATE, DEXTROAMP SULFATE AND AMP SULFATE | amphetamine aspartate; amphetamine sulfate; dextroamphetamine saccharate; dextroamphetamine sulfate | CAPSULE, EXTENDED RELEASE;ORAL | 211546 | ANDA | SpecGx LLC | 0406-0804 | 0406-0804-01 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0406-0804-01) |
Profile for product number 001
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 3.125MG;3.125MG;3.125MG;3.125MG | ||||
Approval Date: | Aug 31, 2023 | TE: | AB2 | RLD: | No |
Profile for product number 002
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 6.25MG;6.25MG;6.25MG;6.25MG | ||||
Approval Date: | Aug 31, 2023 | TE: | AB2 | RLD: | No |
Profile for product number 003
Active Rx/OTC/Discontinued: | RX | Dosage: | CAPSULE, EXTENDED RELEASE;ORAL | Strength | 9.375MG;9.375MG;9.375MG;9.375MG | ||||
Approval Date: | Aug 31, 2023 | TE: | AB2 | RLD: | No |
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