NDC 72162-2176 – Ramelteon

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

Human Prescription Drug

Product NDC72162-2176

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212650
Marketed since
June 30, 2020
Listing expires
December 31, 2026
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (2)

Package NDCDescriptionSince
72162-2176-1100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2176-1)Dec 7, 2023
72162-2176-330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-2176-3)Dec 7, 2023

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