NDC 64764-805 – Rozerem

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

Human Prescription Drug

Product NDC64764-805

Product details

Brand name
Rozerem
Generic name
Ramelteon
Labeler
Takeda Pharmaceuticals America, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021782
Marketed since
July 22, 2005
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Rozerem →

Package NDC codes (2)

Package NDCDescriptionSince
64764-805-10100 TABLET, FILM COATED in 1 BOTTLE (64764-805-10)Jul 22, 2005
64764-805-3030 TABLET, FILM COATED in 1 BOTTLE (64764-805-30)Jul 22, 2005