# Ramelteon

NDC: 71335-1853
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: 20190723

FDA application: ANDA211567

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-1853"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-1853
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bccc4f11-6081-49a1-9abd-2f4c2d69b380