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Ramelteon

NDC 71205-918 · Proficient Rx LP

Generic nameRamelteon
Dosage formTABLET
RouteORAL
Active ingredient(s)RAMELTEON
Strength8 mg/1
Pharmacologic classMelatonin Receptor Agonist [EPC], Melatonin Receptor Agonists [MoA]
Marketing categoryANDA

Packages

71205-918-00 — 100 TABLET in 1 BOTTLE (71205-918-00)

71205-918-30 — 30 TABLET in 1 BOTTLE (71205-918-30)

71205-918-55 — 500 TABLET in 1 BOTTLE (71205-918-55)

71205-918-60 — 60 TABLET in 1 BOTTLE (71205-918-60)

71205-918-72 — 120 TABLET in 1 BOTTLE (71205-918-72)

71205-918-90 — 90 TABLET in 1 BOTTLE (71205-918-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71335-1853 — Ramelteon, 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, +20 more

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