NDC 72189-369 – Ramelteon

Ramelteon 8 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72189-369

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Direct_Rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212650
Marketed since
August 3, 2022
Listing expires
December 31, 2026
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (1)

Package NDCDescriptionSince
72189-369-3030 TABLET, FILM COATED in 1 BOTTLE (72189-369-30)Aug 3, 2022

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