NDC 10135-838 – Ramelteon

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

Human Prescription Drug

Product NDC10135-838

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Marlex Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215435
Marketed since
July 1, 2026
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (2)

Package NDCDescriptionSince
10135-838-01100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-838-01)Jul 1, 2026
10135-838-3030 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (10135-838-30)Jul 1, 2026

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