NDC 76420-628 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC76420-628

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Asclemed USA, Inc.
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 (4)

Package NDCDescriptionSince
76420-628-01100 TABLET in 1 BOTTLE (76420-628-01)Oct 17, 2023
76420-628-3030 TABLET in 1 BOTTLE (76420-628-30)Nov 28, 2023
76420-628-6060 TABLET in 1 BOTTLE (76420-628-60)Nov 28, 2023
76420-628-9090 TABLET in 1 BOTTLE (76420-628-90)Nov 28, 2023

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