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Ramelteon

NDC 70700-272 · Xiromed, 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

70700-272-05 — 500 TABLET, FILM COATED in 1 BOTTLE (70700-272-05)

70700-272-10 — 100 TABLET, FILM COATED in 1 BOTTLE (70700-272-10)

70700-272-30 — 30 TABLET, FILM COATED in 1 BOTTLE (70700-272-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42571-375 — Ramelteon, 50268-822 — Ramelteon, 51407-523 — Ramelteon, 52817-235 — Ramelteon, 59651-505 — RAMELTEON, 60687-692 — Ramelteon, 63629-8531 — Ramelteon, 64764-805 — ramelteon, 70010-028 — Ramelteon, 70518-4257 — Ramelteon, 70710-1344 — Ramelteon, 70771-1495 — Ramelteon, 71205-918 — Ramelteon, 71335-1853 — Ramelteon, 71335-2186 — Ramelteon, 71335-2310 — Ramelteon, 71335-2411 — RAMELTEON, 71335-2886 — Ramelteon, 72162-2161 — Ramelteon, 72162-2169 — 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.