NDC 50268-822 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC50268-822

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
AvPAK
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA215243
Marketed since
May 20, 2026
Listing expires
December 31, 2027
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (1)

Package NDCDescriptionSince
50268-822-1550 BLISTER PACK in 1 BOX (50268-822-15) / 1 TABLET in 1 BLISTER PACK (50268-822-11)May 20, 2026

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