Drugplain

RAMELTEON 8 mg/1

RAMELTEON · TABLET, FILM COATED · Bryant Ranch Prepack

No Recall History
Plain English

RAMELTEON is a tablet, film coated containing ramelteon at 8 mg/1, taken oral. Manufactured by Bryant Ranch Prepack.

Key Facts

Brand Name
RAMELTEON
Generic Name
RAMELTEON
NDC Code (Product)
71335-2411
Manufacturer
Bryant Ranch Prepack
Strength
8 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA215972
Drug Class
Melatonin Receptor Agonist [EPC]
Marketing Start
07/10/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective72 reports
off label use68 reports
nausea63 reports
decreased appetite60 reports
diarrhoea59 reports
insomnia58 reports
fatigue53 reports
pneumonia49 reports
fall47 reports
anaemia42 reports

Frequently Asked Questions

What is RAMELTEON used for?

RAMELTEON contains RAMELTEON. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is RAMELTEON a controlled substance?

RAMELTEON is not classified as a controlled substance by the DEA.

What is the generic name for RAMELTEON?

The generic name for RAMELTEON is RAMELTEON. There are 11 other brand versions of RAMELTEON.

What is the NDC code for RAMELTEON 8 mg/1?

The NDC (National Drug Code) for RAMELTEON 8 mg/1 is 71335-2411, listed by Bryant Ranch Prepack.

Product NDC

71335-2411

Package NDC

71335-2411-1

Other RAMELTEON Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)