RAMELTEON 8 mg/1
RAMELTEON · TABLET · DIRECT RX
No Recall History
Plain English
RAMELTEON is a tablet containing ramelteon at 8 mg/1, taken oral. Manufactured by DIRECT RX.
Key Facts
- Brand Name
- RAMELTEON
- Generic Name
- RAMELTEON
- NDC Code (Product)
72189-153- Manufacturer
- DIRECT RX
- Strength
- 8 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- ANDA211567
- Drug Class
- Melatonin Receptor Agonist [EPC]
- Marketing Start
- 11/03/2020
Recall History
No Recall HistorySide 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 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 72189-153, listed by DIRECT RX.