NDC 70710-1344 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70710-1344

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Zydus Pharmaceuticals USA Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA211567
Marketed since
July 23, 2019
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
70710-1344-1100 TABLET in 1 BOTTLE (70710-1344-1)Jul 23, 2019
70710-1344-330 TABLET in 1 BOTTLE (70710-1344-3)Jul 23, 2019
70710-1344-5500 TABLET in 1 BOTTLE (70710-1344-5)Jul 23, 2019

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