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Dextroamphetamine saccharate, amphetamine aspartate monohydrate, dextroamphetamine sulfate, amphetamine sulfate

Active substance: DEXTROAMPHETAMINE SACCHARATE, AMPHETAMINE ASPARTATE MONOHYDRATE, DEXTROAMPHETAMINE SULFATE, AMPHETAMINE SULFATE

CAPSULE, EXTENDED RELEASE · DEXTROAMPHETAMINE SACCHARATE 9.375 mg/1, AMPHETAMINE ASPARTATE MONOHYDRATE 9.375 mg/1, DEXTROAMPHETAMINE SULFATE 9.375 mg/1, AMPHETAMINE SULFATE 9.375 mg/1

United StatesActive

Marketing holder: Sun Pharmaceutical Industries, Inc.

Verified 2026-10-09 · openFDA NDC

Registration
Registration number
57664-952
Registration status
Active
Dispensing
Prescription only
Control marker
CII
Route
ORAL
Sources
  • product · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source
  • ingredients.1 · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source
  • ingredients.2 · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source
  • ingredients.3 · openFDA NDC · 57664-952 · Verified 2026-10-09 · open in source