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DEXMETHYLPHENIDATE HYDROCHLORIDE

Active substance: dexmethylphenidate

CAPSULE, EXTENDED RELEASE · DEXMETHYLPHENIDATE HYDROCHLORIDE 40 mg/1

United StatesActive

Marketing holder: Granules Pharmaceuticals Inc.

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United StatescontrolledSchedule: CII

    Source: openFDA NDC · record 01a1208c-294b-7a8c-8a43-4b7763c3faf5,01a1208c-2ccf-7dcb-8f93-39ec5c7d93f3,01a1208c-4698-7b3c-a135-6d84ffe9a739,01a1208c-4816-7ba5-a5a7-4a55c4099c0e,01a1208c-4f2f-760d-8c80-37c2cabc10fc;count=114 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
70010-011
Registration status
Active
Dispensing
Prescription only
Control marker
CII
Route
ORAL
Sources
  • product · openFDA NDC · 70010-011 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 70010-011 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 70010-011 · Verified 2026-10-09 · open in source