NDC 70700-272 – Ramelteon

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

Human Prescription Drug

Product NDC70700-272

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Xiromed, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216209
Marketed since
November 25, 2022
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
70700-272-05500 TABLET, FILM COATED in 1 BOTTLE (70700-272-05)Nov 25, 2022
70700-272-10100 TABLET, FILM COATED in 1 BOTTLE (70700-272-10)Nov 25, 2022
70700-272-3030 TABLET, FILM COATED in 1 BOTTLE (70700-272-30)Nov 25, 2022

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