# Ramelteon

NDC: 10135-838
Generic name: Ramelteon
Labeler / Manufacturer: Marlex Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260701

FDA application: ANDA215435

## 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:"10135-838"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=10135-838
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=56d1ac8d-5131-4eed-e063-6294a90a402e