Ramelteon

NDC 0832-1250 · Upsher-Smith Laboratories, 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

0832-1250-11 — 100 TABLET, FILM COATED in 1 BOTTLE (0832-1250-11)

0832-1250-30 — 30 TABLET, FILM COATED in 1 BOTTLE (0832-1250-30)

FDA lists these products with the same active ingredient.

0591-2191 — Ramelteon, 0904-7494 — Ramelteon, 10135-838 — Ramelteon, 42291-776 — Ramelteon, 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, 70700-272 — Ramelteon, 70710-1344 — Ramelteon, 70771-1495 — Ramelteon, 71205-918 — Ramelteon, 71335-1853 — Ramelteon, 71335-2186 — 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.