# Ramelteon

NDC: 70010-028
Generic name: Ramelteon
Labeler / Manufacturer: Granules Pharmaceuticals Inc.
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:"70010-028"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70010-028
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a0a57843-81cb-474d-8e90-e04bbe93216a