NDC 71205-918 – Ramelteon

Ramelteon 8 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-918

Product details

Brand name
Ramelteon
Generic name
Ramelteon
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213186
Marketed since
October 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
Melatonin Receptor Agonist

Active ingredients

Uses, dosage, side effects and warnings for Ramelteon →

Package NDC codes (6)

Package NDCDescriptionSince
71205-918-00100 TABLET in 1 BOTTLE (71205-918-00)Jul 7, 2021
71205-918-3030 TABLET in 1 BOTTLE (71205-918-30)Jul 7, 2021
71205-918-55500 TABLET in 1 BOTTLE (71205-918-55)Jul 7, 2021
71205-918-6060 TABLET in 1 BOTTLE (71205-918-60)Jul 7, 2021
71205-918-72120 TABLET in 1 BOTTLE (71205-918-72)Jul 7, 2021
71205-918-9090 TABLET in 1 BOTTLE (71205-918-90)Jul 7, 2021

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