# Ramelteon

NDC: 72319-005
Generic name: Ramelteon
Labeler / Manufacturer: i3 Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200430

FDA application: ANDA212650

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72319-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72319-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=32c52e03-4c2e-4774-9397-f1f0ee99b320