# RAMELTEON

NDC: 76420-880
Generic name: RAMELTEON
Labeler / Manufacturer: Asclemed USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230710

FDA application: ANDA215972

## 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:"76420-880"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=76420-880
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8213998f-9a14-4ebb-a87a-4f33416dfb21