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Ramelteon

Active substance: ramelteon

TABLET, FILM COATED · RAMELTEON 8 mg/1

United StatesActive

Marketing holder: Upsher-Smith Laboratories, LLC

Verified 2026-10-09 · openFDA NDC

Composition
Import and control

Control by country

  • United Statesprescription only

    Source: openFDA NDC · record 01a1208c-2b43-7268-ba4a-d24e96a70458,01a1208c-34bc-7182-9900-45c0ff0e19b8,01a1208c-dcc2-711d-a5aa-171a3ebfc148,01a1208d-c902-7658-81de-2e608ce0f5a6,01a1208d-e7a9-7ede-abff-a48ad97ce69a;count=41 · valid from 2026-10-09 · verified 2026-10-09

More on control status
Registration
Registration number
0832-1250
Registration status
Active
Dispensing
Prescription only
Route
ORAL
Sources
  • product · openFDA NDC · 0832-1250 · Verified 2026-10-09 · open in source
  • registration_status · openFDA NDC · 0832-1250 · Verified 2026-10-09 · open in source
  • ingredients.0 · openFDA NDC · 0832-1250 · Verified 2026-10-09 · open in source