# Ramelteon

NDC: 55700-874
Generic name: Ramelteon
Labeler / Manufacturer: Quality Care Products, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200728
Marketing ended: 20260531
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:"55700-874"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55700-874
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=316b5aa6-46dd-4808-b30d-b36fc730adbc