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Cevimeline Hydrochloride

Active substance: cevimeline

CAPSULE · CEVIMELINE HYDROCHLORIDE 30 mg/1

United StatesActive

Marketing holder: Viona Pharmaceuticals Inc

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-5893-76dc-8a70-cdf3bde40acc,01a1208c-b652-7aa3-8303-f90b24d1abb8,01a1208c-e20f-7f87-a378-4284284d05c5,01a1208d-9b85-7dac-81eb-db755b841c4b,01a1208e-aa47-74fa-8c1e-f16aa115b122;count=22 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
72578-208
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 72578-208 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 72578-208 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 72578-208 · Verified 2026-10-09 · open in source