NDC 0591-2191 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC0591-2191

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Actavis Pharma, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA091610
Marketed since
July 22, 2019
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
0591-2191-01100 TABLET in 1 BOTTLE (0591-2191-01)Jul 22, 2019
0591-2191-3030 TABLET in 1 BOTTLE (0591-2191-30)Jul 22, 2019

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