Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate, and amphetamine sulfate
Active substance: DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE
TABLET · DEXTROAMPHETAMINE SACCHARATE 2.5 mg/1, AMPHETAMINE ASPARTATE 2.5 mg/1, DEXTROAMPHETAMINE SULFATE 2.5 mg/1, AMPHETAMINE SULFATE 2.5 mg/1
United StatesActive
Marketing holder: Sun Pharmaceutical Industries, Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- DEXTROAMPHETAMINE SACCHARATE · 2.5 mg/1
- AMPHETAMINE ASPARTATE · 2.5 mg/1
- DEXTROAMPHETAMINE SULFATE · 2.5 mg/1
- AMPHETAMINE SULFATE · 2.5 mg/1
Registration
- Registration number
- 57664-643
- Registration status
- Active
- Dispensing
- Prescription only
- Control marker
- CII
- Route
- ORAL
Sources
- product · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source
- ingredients.1 · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source
- ingredients.2 · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source
- ingredients.3 · openFDA NDC · 57664-643 · Verified 2026-10-09 · open in source