NDC 71335-1853 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1853

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211567
Marketed since
July 23, 2019
Listing expires
December 31, 2026
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (1)

Package NDCDescriptionSince
71335-1853-130 TABLET in 1 BOTTLE (71335-1853-1)Dec 21, 2021

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