NDC 72319-005 – Ramelteon

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

Human Prescription Drug

Product NDC72319-005

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
i3 Pharmaceuticals, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA212650
Marketed since
April 30, 2020
Listing expires
December 31, 2026
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (3)

Package NDCDescriptionSince
72319-005-0130 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-01)Apr 30, 2020
72319-005-04100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-04)Apr 30, 2020
72319-005-05500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72319-005-05)Apr 30, 2020

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