# Ramelteon

NDC: 52817-235
Generic name: Ramelteon
Labeler / Manufacturer: TruPharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200630

FDA application: ANDA212650

## Active ingredients

- RAMELTEON: 8 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52817-235"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-235
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3d0cc378-4bc5-425c-8f41-43eb734c24d9