Ramelteon

NDC 80425-0343 · Advanced Rx Pharmacy of Tennessee, LLC

Generic nameRamelteon

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)RAMELTEON

Strength8 mg/1

Pharmacologic classMelatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]

Marketing categoryANDA

Packages

80425-0343-1 — 30 TABLET, FILM COATED in 1 BOTTLE (80425-0343-1)

FDA lists these products with the same active ingredient.

71335-2186 — Ramelteon, 71335-2310 — Ramelteon, 71335-2411 — RAMELTEON, 71335-2886 — Ramelteon, 72162-2161 — Ramelteon, 72162-2169 — Ramelteon, 72162-2176 — Ramelteon, 72162-2644 — Ramelteon, 72189-153 — RAMELTEON, 72189-369 — Ramelteon, 72189-484 — Ramelteon, 72319-005 — Ramelteon, 76420-628 — Ramelteon, 76420-880 — RAMELTEON, 80425-0203 — Ramelteon, 80425-0593 — Ramelteon, 82804-216 — Ramelteon, 85742-023 — Ramelteon, 85766-251 — Ramelteon, 87063-189 — Ramelteon, +20 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.