# Ramelteon

NDC: 71205-918
Generic name: Ramelteon
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20201001

FDA application: ANDA213186

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-918"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-918
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ca849d3-f0ba-45b5-9aec-f4b7ea105fac