NDC 71335-2411 – Ramelteon

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

Human Prescription Drug

Product NDC71335-2411

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215972
Marketed since
July 10, 2023
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
71335-2411-130 TABLET, FILM COATED in 1 BOTTLE (71335-2411-1)Jun 10, 2024
71335-2411-260 TABLET, FILM COATED in 1 BOTTLE (71335-2411-2)Jun 10, 2024

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