# Ramelteon

NDC: 72162-2169
Generic name: Ramelteon
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190722

FDA application: ANDA091693

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72162-2169"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2169
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=57536bd9-7dfa-4be5-854a-95fea43d54bc