NDC 72162-2161 – Ramelteon

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

Human Prescription Drug

Product NDC72162-2161

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213815
Marketed since
October 26, 2020
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (1)

Package NDCDescriptionSince
72162-2161-330 TABLET, FILM COATED in 1 BOTTLE (72162-2161-3)Oct 26, 2020

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