NDC 70518-4257 – Ramelteon

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

Human Prescription Drug

Product NDC70518-4257

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
REMEDYREPACK INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA213815
Marketed since
January 20, 2025
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
70518-4257-030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4257-0)Jan 20, 2025

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