NDC 87063-189 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC87063-189

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
ASCLEMED USA INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215243
Marketed since
May 1, 2023
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (7)

Package NDCDescriptionSince
87063-189-01100 TABLET in 1 BOTTLE (87063-189-01)May 7, 2026
87063-189-055 TABLET in 1 BOTTLE (87063-189-05)May 7, 2026
87063-189-1010 TABLET in 1 BOTTLE (87063-189-10)May 7, 2026
87063-189-2020 TABLET in 1 BOTTLE (87063-189-20)May 7, 2026
87063-189-3030 TABLET in 1 BOTTLE (87063-189-30)May 7, 2026
87063-189-6060 TABLET in 1 BOTTLE (87063-189-60)May 7, 2026
87063-189-9090 TABLET in 1 BOTTLE (87063-189-90)May 7, 2026

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