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Amoxapine

Active substance: amoxapine

TABLET · AMOXAPINE 150 mg/1

United StatesActive

Marketing holder: Actavis Pharma, Inc.

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-d479-7979-a349-beae9a30bd9a,01a1208d-c4d6-740b-912b-53e9bc875196,01a1208e-9a73-7686-9460-c79a0a361f12,01a12090-fb9c-71b0-8b89-022775b93180,01a12092-1698-72e2-a4d4-230545990800;count=8 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0591-5716
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0591-5716 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0591-5716 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0591-5716 · Verified 2026-10-09 · open in source