NDC 71335-2186 – Ramelteon

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

Human Prescription Drug

Product NDC71335-2186

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
71335-2186-130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-1)Nov 4, 2022
71335-2186-260 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-2186-2)Nov 4, 2022

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