NDC 72189-153 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC72189-153

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
DIRECT RX
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211567
Marketed since
November 3, 2020
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
72189-153-3030 TABLET in 1 BOTTLE (72189-153-30)Nov 3, 2020

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