DEXMETHYLPHENIDATE HYDROCHLORIDE
Active substance: dexmethylphenidate
CAPSULE, EXTENDED RELEASE · DEXMETHYLPHENIDATE HYDROCHLORIDE 35 mg/1
United StatesActive
Marketing holder: Granules Pharmaceuticals Inc.
Verified 2026-10-09 · openFDA NDC
- Source: openFDA NDC
- Countries with the substance registered: 1
Composition
- DEXMETHYLPHENIDATE HYDROCHLORIDE · 35 mg/1
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
Registration
- Registration number
- 70010-010
- Registration status
- Active
- Dispensing
- Prescription only
- Control marker
- CII
- Route
- ORAL
Sources
- product · openFDA NDC · 70010-010 · Verified 2026-10-09 · open in source
- registration_status · openFDA NDC · 70010-010 · Verified 2026-10-09 · open in source
- ingredients.0 · openFDA NDC · 70010-010 · Verified 2026-10-09 · open in source